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Cytopenia - NOT Fanconi anaemia v4.31 RPL17 Achchuthan Shanmugasundram Added comment: Comment on phenotypes: This gene has now been associated with relevant phenotype in OMIM (MIM #621262) and this OMIM record was last accessed on 20 January 2026.
Cytopenia - NOT Fanconi anaemia v4.31 RPL17 Achchuthan Shanmugasundram Phenotypes for gene: RPL17 were changed from Diamond-Blackfan anemia, MONDO:0015253 to Diamond-Blackfan anemia 22, OMIM:621262; Diamond-Blackfan anemia 22, MONDO:0979244
Cytopenia - NOT Fanconi anaemia v4.30 RPL17 Achchuthan Shanmugasundram edited their review of gene: RPL17: Changed phenotypes to: Diamond-Blackfan anemia 22, OMIM:621262, Diamond-Blackfan anemia 22, MONDO:0979244
Cytopenia - NOT Fanconi anaemia v4.30 RPL27 Achchuthan Shanmugasundram Tag Q2_25_ promote_green was removed from gene: RPL27.
Tag Q2_25_ NHS_review was removed from gene: RPL27.
Cytopenia - NOT Fanconi anaemia v4.30 RPL17 Achchuthan Shanmugasundram Tag Q2_25_ promote_green was removed from gene: RPL17.
Cytopenia - NOT Fanconi anaemia v4.30 FASLG Achchuthan Shanmugasundram Tag Q2_25_ promote_green was removed from gene: FASLG.
Cytopenia - NOT Fanconi anaemia v4.30 FAS Achchuthan Shanmugasundram Tag Q2_25_ promote_green was removed from gene: FAS.
Cytopenia - NOT Fanconi anaemia v4.30 RPL27 Achchuthan Shanmugasundram edited their review of gene: RPL27: Added comment: The rating of this gene has been updated to green following NHS Genomic Medicine Service approval.; Changed rating: GREEN
Cytopenia - NOT Fanconi anaemia v4.30 RPL17 Achchuthan Shanmugasundram commented on gene: RPL17: The rating of this gene has been updated to green following NHS Genomic Medicine Service approval.
Cytopenia - NOT Fanconi anaemia v4.30 FASLG Achchuthan Shanmugasundram commented on gene: FASLG: The rating of this gene has been updated to green and the mode of inheritance updated to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Cytopenia - NOT Fanconi anaemia v4.30 FAS Achchuthan Shanmugasundram commented on gene: FAS: The rating of this gene has been updated to green and the mode of inheritance updated to BOTH monoallelic and biallelic, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Cytopenia - NOT Fanconi anaemia v4.29 RPL27 Achchuthan Shanmugasundram Source Expert Review Green was added to RPL27.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v4.29 RPL17 Achchuthan Shanmugasundram Source Expert Review Green was added to RPL17.
Source NHS GMS was added to RPL17.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v4.29 FASLG Achchuthan Shanmugasundram Source Expert Review Green was added to FASLG.
Source NHS GMS was added to FASLG.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v4.29 FAS Achchuthan Shanmugasundram Source Expert Review Green was added to FAS.
Source NHS GMS was added to FAS.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v4.28 SRP72 Arina Puzriakova Phenotypes for gene: SRP72 were changed from Inherited Bone Marrow Failure Syndromes - Aplastic Anaemia; Bone marrow failure, familial, 614675; Familial MDS (Myelodysplastic syndromes); Bone Marrow Failure, Familial; 614675 Bone marrow failure syndrome 1; Familial Bone Marrow Failure to Bone marrow failure syndrome 1, OMIM:614675; autosomal dominant aplasia and myelodysplasia, MONDO:0013851
Cytopenia - NOT Fanconi anaemia v4.27 SRP72 Arina Puzriakova Publications for gene: SRP72 were set to 22541560; 29146883
Cytopenia - NOT Fanconi anaemia v4.26 SRP72 Arina Puzriakova Classified gene: SRP72 as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v4.26 SRP72 Arina Puzriakova Added comment: Comment on list classification: Several lines of conflicting evidence, including lack of relevant phenotype in mouse model, unaffected carriers and variants in other genes that could explain patient phenotypes - this means strongly corroborating evidence is required before this gene can be added to a diagnostic panel.
Cytopenia - NOT Fanconi anaemia v4.26 SRP72 Arina Puzriakova Gene: srp72 has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v4.25 SRP72 Arina Puzriakova reviewed gene: SRP72: Rating: AMBER; Mode of pathogenicity: None; Publications: 22541560, 29146883, 32098966, 31254415, 40922878; Phenotypes: Bone marrow failure syndrome 1, OMIM:614675, autosomal dominant aplasia and myelodysplasia, MONDO:0013851; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v4.25 RAP1B Arina Puzriakova Phenotypes for gene: RAP1B were changed from Syndromic intellectual disability; cytopenia to Thrombocytopenia 11 with multiple congenital anomalies and dysmorphic facies, OMIM:620654; Syndromic intellectual disability; Cytopenia
Cytopenia - NOT Fanconi anaemia v4.24 SLC46A1 Arina Puzriakova Classified gene: SLC46A1 as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v4.24 SLC46A1 Arina Puzriakova Added comment: Comment on list classification: There is sufficient evidence to promote this gene to Green. At least 5 unrelated individuals with biallelic variants in this gene and hereditary folate malabsorption which can progress to severe pancytopenia (PMID: 11807405; 17446347; 21333572; 40937236). This is a key feature of this condition and warrants inclusion on the panel.
Cytopenia - NOT Fanconi anaemia v4.24 SLC46A1 Arina Puzriakova Gene: slc46a1 has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v4.23 SLC46A1 Arina Puzriakova Tag Q3_25_promote_green tag was added to gene: SLC46A1.
Tag Q3_25_NHS_review tag was added to gene: SLC46A1.
Cytopenia - NOT Fanconi anaemia v4.23 SLC46A1 Arina Puzriakova Entity copied from Cytopenias and congenital anaemias v1.119
Cytopenia - NOT Fanconi anaemia v4.23 SLC46A1 Arina Puzriakova gene: SLC46A1 was added
gene: SLC46A1 was added to Cytopenia - NOT Fanconi anaemia. Sources: Expert Review,Literature
Mode of inheritance for gene: SLC46A1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: SLC46A1 were set to 21333572; 17446347; 29390264; 11804211; 17641272
Phenotypes for gene: SLC46A1 were set to Folate malabsorption, hereditary, OMIM:229050; anemia; pancytopenia
Cytopenia - NOT Fanconi anaemia v4.22 EFL1 Arina Puzriakova Phenotypes for gene: EFL1 were changed from Shwachman-Diamond syndrome 2, 617941; 617941 Shwachman-Diamond syndrome 2 to Shwachman-Diamond syndrome 2, OMIM:617941
Cytopenia - NOT Fanconi anaemia v4.21 CSF3R Arina Puzriakova Phenotypes for gene: CSF3R were changed from Neutropenia, severe congenital, 7, autosomal recessive, 617014; 617014 Neutropenia, severe congenital, 7; 617014 Neutropenia, severe congenital, 7, autosomal recessive; Severe congenital neutropenia to Neutropenia, severe congenital, 7, autosomal recessive, OMIM:617014
Cytopenia - NOT Fanconi anaemia v4.20 RPL26 Achchuthan Shanmugasundram Classified gene: RPL26 as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v4.20 RPL26 Achchuthan Shanmugasundram Added comment: Comment on list classification: Although there are five unrelated families reported with monoallelic RPL26 variants in total (PMIDs: 22431104 & 39268718), only two unrelated individuals have been reported with cytopenia. Hence, this gene can only be rated amber with current evidence.
Cytopenia - NOT Fanconi anaemia v4.20 RPL26 Achchuthan Shanmugasundram Gene: rpl26 has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v4.19 RPL26 Achchuthan Shanmugasundram Phenotypes for gene: RPL26 were changed from ?Diamond-Blackfan anemia 11, 614900 to ?Diamond-Blackfan anemia 11, OMIM:614900
Cytopenia - NOT Fanconi anaemia v4.18 RPL26 Achchuthan Shanmugasundram Publications for gene: RPL26 were set to
Cytopenia - NOT Fanconi anaemia v4.17 RPL26 Achchuthan Shanmugasundram Mode of inheritance for gene: RPL26 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v4.16 RPL26 Achchuthan Shanmugasundram reviewed gene: RPL26: Rating: AMBER; Mode of pathogenicity: None; Publications: 39268718; Phenotypes: ?Diamond-Blackfan anemia 11, OMIM:614900; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v4.16 RPL17 Achchuthan Shanmugasundram Classified gene: RPL17 as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v4.16 RPL17 Achchuthan Shanmugasundram Added comment: Comment on list classification: As reviewed by Dmitrijs Rots, there are two unrelated pedigrees and functional evidence available in support of the association of this gene to phenotype. Hence, this can be promoted to green rating in the next GMS update.
Cytopenia - NOT Fanconi anaemia v4.16 RPL17 Achchuthan Shanmugasundram Gene: rpl17 has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v4.15 RPL17 Achchuthan Shanmugasundram Phenotypes for gene: RPL17 were changed from Diamond-Blackfan anemia to Diamond-Blackfan anemia, MONDO:0015253
Cytopenia - NOT Fanconi anaemia v4.14 RPL17 Achchuthan Shanmugasundram Tag Q2_25_ promote_green tag was added to gene: RPL17.
Cytopenia - NOT Fanconi anaemia v4.14 RPL17 Achchuthan Shanmugasundram reviewed gene: RPL17: Rating: GREEN; Mode of pathogenicity: None; Publications: 39088281; Phenotypes: Diamond-Blackfan anemia, MONDO:0015253; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v4.14 CASP10 Achchuthan Shanmugasundram Classified gene: CASP10 as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v4.14 CASP10 Achchuthan Shanmugasundram Added comment: Comment on list classification: Despite sufficient cases being reported with the phenotype, the presence of identified variants in healthy individuals, reduced segregation of variants with the disease, inconsistencies in the reported phenotypes across cases with the same variants, and normal FAS-mediated apoptosis with variants from affected individuals suggest that this gene should not be promoted to green rating.
Cytopenia - NOT Fanconi anaemia v4.14 CASP10 Achchuthan Shanmugasundram Gene: casp10 has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v4.13 CASP10 Achchuthan Shanmugasundram Classified gene: CASP10 as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v4.13 CASP10 Achchuthan Shanmugasundram Gene: casp10 has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v4.12 CASP10 Achchuthan Shanmugasundram Publications for gene: CASP10 were set to
Cytopenia - NOT Fanconi anaemia v4.11 CASP10 Achchuthan Shanmugasundram Phenotypes for gene: CASP10 were changed from ALPS to Autoimmune lymphoproliferative syndrome, type II, OMIM:603909
Cytopenia - NOT Fanconi anaemia v4.10 CASP10 Achchuthan Shanmugasundram Mode of inheritance for gene: CASP10 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v4.9 CASP10 Achchuthan Shanmugasundram commented on gene: CASP10: PMID:34329798 - Two patients were identified with heterozygous p.Ile406Leu variant and one was identified with p.Cys401LeufsTer15 variant. The p.Ile406Leu variant did not segregate with the disease, while the family of the patient with p.Cys401LeufsTer15 variant was not studied. The p.Ile406Leu variant, which was previously reported in several cases was found at an allele frequency of 2% in healthy individuals in certain ethnicities from the 1000 genomes database. In addition, functional assays did not show any impairment in one of these patients and five previously reported patients in comparison to healthy donors. Although p.Cys401LeufsTer15 variant was classified as likely pathogenic, it is also proposed that it is not per se causative of disease as the variant is present at higher than expected allele frequency in healthy individuals. There is also significant differences in the clinical presentations with the patient with this variant in this publication and a previously reported patient within the same variant. Another previously reported variant, p.Tyr446Cys was also present at an allele frequency of 4% in healthy individuals from 1000 genomes database, and p.Val410Ile was discarded as disease-causing by the same authors.

PMID:38704374 aimed to assess the impact of CASP10 variants on ALPS pathogenesis. Using a large cohort dataset, the authors were able to confirm that the missense variants p.Val410Ile and p.Tyr446Cys, are present in the general population at a high frequency. Furthermore, these variants do not affect the CASP10 catalytic domain and no difference was observed in CASP10 protein expression or FAS-mediated apoptosis between healthy controls and subjects bearing these variants in both homozygous and heterozygous states. Two patient had the CASP10 variant p.Cys401LeufsTer15, which lies within QACQG catalytic site in the CASP10 catalytic domain. One of the two patients was homozygous for this variant, resulting in a lack of Caspase-10 RNA and protein. However, it was reported that FAS-mediated apoptosis was comparable to healthy controls in each of the tested cell lines suspected to have a role in ALPS. In the other patient, who was heterozygous p.Cys401LeufsTer15, the authors report that although the levels of CASP10 protein expression was reduced, there was normal FAS-mediated apoptosis compared to healthy controls. From these results, it was concluded that Caspase-10 is dispensable for FAS-mediated apoptosis and an undetectable CASP10 protein expression has no impact on lymphocyte apoptosis and on individuals’ clinical and laboratory phenotype. It is also commented that post-translational or epigenetic mechanisms may play a role and yet unidentified.
Cytopenia - NOT Fanconi anaemia v4.9 CASP10 Achchuthan Shanmugasundram reviewed gene: CASP10: Rating: AMBER; Mode of pathogenicity: None; Publications: 34329798, 38704374; Phenotypes: Autoimmune lymphoproliferative syndrome, type II, OMIM:603909; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v4.9 FASLG Achchuthan Shanmugasundram Classified gene: FASLG as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v4.9 FASLG Achchuthan Shanmugasundram Added comment: Comment on list classification: There is sufficient evidence available for the association of both monoallelic and biallelic FASLG variants with ALPS, which has cytopenia as presenting phenotype. Hence, this gene can be promoted to green rating in the next GMS update.
Cytopenia - NOT Fanconi anaemia v4.9 FASLG Achchuthan Shanmugasundram Gene: faslg has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v4.8 FASLG Achchuthan Shanmugasundram Tag Q2_25_ promote_green tag was added to gene: FASLG.
Cytopenia - NOT Fanconi anaemia v4.8 FASLG Achchuthan Shanmugasundram Phenotypes for gene: FASLG were changed from ALPS to Autoimmune lymphoproliferative syndrome, type IB, OMIM:601859
Cytopenia - NOT Fanconi anaemia v4.7 FASLG Achchuthan Shanmugasundram Publications for gene: FASLG were set to
Cytopenia - NOT Fanconi anaemia v4.6 FASLG Achchuthan Shanmugasundram Mode of inheritance for gene: FASLG was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v4.5 FASLG Achchuthan Shanmugasundram reviewed gene: FASLG: Rating: GREEN; Mode of pathogenicity: None; Publications: 8787672, 16627752, 17605793, 25451160, 26334989; Phenotypes: Autoimmune lymphoproliferative syndrome, type IB, OMIM:601859; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v4.5 FAS Achchuthan Shanmugasundram changed review comment from: FAS has a well-established gene-disease association for autosomal dominant autoimmune lymphoproliferative syndrome (ALPS) in OMIM (MIM #601859) and Gene2Phenotype (with 'definitive' rating on 'Skin disorders' panel). OMIM also reported autoimmune hemolytic anemia, thrombocytopenia and neutropenia as clinical presentations of this disorder.

This gene has also been associated with biallelic ALPS syndrome in Gene2Phenotype (with 'definitive' rating on 'Skin disorders' panel).

PMID:34171534 reviewed evidence from previously published reports, which showed that there is sufficient evidence available for the association of both monoallelic and biallelic germline variants with ALPS syndrome. There is also sufficient evidence available for the presence of autoimmune cytopenias (hemolytic anemia, thrombocytopenia and neutropenia) in both patients with both monoallelic and biallelic variants.; to: FAS has a well-established gene-disease association for autoimmune lymphoproliferative syndrome (ALPS). Both germline and somatic variants have been reported to cause ALPS.

FAS has been associated with autosomal dominant ALPS in OMIM (MIM #601859) and Gene2Phenotype (with 'definitive' rating on 'Skin disorders' panel). OMIM also reports autoimmune hemolytic anemia, thrombocytopenia and neutropenia as clinical presentations of this disorder.

This gene has also been associated with autosomal recessive ALPS syndrome in Gene2Phenotype (with 'definitive' rating on 'Skin disorders' panel).

PMID:34171534 reviewed evidence from previously published reports, which showed that there is sufficient evidence available for the association of both monoallelic and biallelic germline variants with ALPS syndrome. There is also sufficient evidence available for the presence of autoimmune cytopenias (hemolytic anemia, thrombocytopenia and neutropenia) in both patients with both monoallelic and biallelic variants.
Cytopenia - NOT Fanconi anaemia v4.5 FAS Achchuthan Shanmugasundram Classified gene: FAS as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v4.5 FAS Achchuthan Shanmugasundram Added comment: Comment on list classification: There is sufficient evidence available for the association of both monoallelic and biallelic variants with autoimmune cytopenia. Hence, this gene can be promoted to green rating in the next GMS update.
Cytopenia - NOT Fanconi anaemia v4.5 FAS Achchuthan Shanmugasundram Gene: fas has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v4.4 FAS Achchuthan Shanmugasundram Phenotypes for gene: FAS were changed from ALPS to Autoimmune lymphoproliferative syndrome, type IA, OMIM:601859
Cytopenia - NOT Fanconi anaemia v4.3 FAS Achchuthan Shanmugasundram Publications for gene: FAS were set to
Cytopenia - NOT Fanconi anaemia v4.2 FAS Achchuthan Shanmugasundram Mode of inheritance for gene: FAS was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v4.1 FAS Achchuthan Shanmugasundram Tag Q2_25_ promote_green tag was added to gene: FAS.
Cytopenia - NOT Fanconi anaemia v4.1 FAS Achchuthan Shanmugasundram reviewed gene: FAS: Rating: GREEN; Mode of pathogenicity: None; Publications: 34171534; Phenotypes: Autoimmune lymphoproliferative syndrome, type IA, OMIM:601859; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v4.1 Sarah Leigh Panel version 4.0 has been signed off on 2025-04-30
Cytopenia - NOT Fanconi anaemia v4.0 Sarah Leigh promoted panel to version 4.0
Cytopenia - NOT Fanconi anaemia v3.39 RPL27 Sarah Leigh Tag Q2_25_ promote_green tag was added to gene: RPL27.
Tag Q2_25_ NHS_review tag was added to gene: RPL27.
Cytopenia - NOT Fanconi anaemia v3.39 RPL27 Sarah Leigh reviewed gene: RPL27: Rating: GREEN; Mode of pathogenicity: None; Publications: 25424902, 38988374; Phenotypes: ?Diamond-Blackfan anemia 16, OMIM:617408, Diamond-Blackfan anemia 16, MONDO:0044309; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v3.39 RPL27 Sarah Leigh Publications for gene: RPL27 were set to 25424902; 38988374
Cytopenia - NOT Fanconi anaemia v3.38 RPL27 Sarah Leigh Phenotypes for gene: RPL27 were changed from Diamond-Blackfan anemia; ?Diamond-Blackfan anemia 16, 617408 to ?Diamond-Blackfan anemia 16, OMIM:617408; Diamond-Blackfan anemia 16, MONDO:0044309
Cytopenia - NOT Fanconi anaemia v3.37 RPL27 Sarah Leigh Publications for gene: RPL27 were set to 25424902
Cytopenia - NOT Fanconi anaemia v3.36 RPL26 Dmitrijs Rots reviewed gene: RPL26: Rating: GREEN; Mode of pathogenicity: None; Publications: 39268718; Phenotypes: Diamond-Blackfan anemia; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v3.36 RPL17 Dmitrijs Rots gene: RPL17 was added
gene: RPL17 was added to Cytopenia - NOT Fanconi anaemia. Sources: Literature
Mode of inheritance for gene: RPL17 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: RPL17 were set to 39088281
Phenotypes for gene: RPL17 were set to Diamond-Blackfan anemia
Penetrance for gene: RPL17 were set to Incomplete
Review for gene: RPL17 was set to GREEN
Added comment: PMID: 39088281 described 2 families with Diamond-Blackfan anemia & functional data. Enough evidence for the green rating.
probably gene should be added also to other panels (like limb disorders; hematological malignancies).
Sources: Literature
Cytopenia - NOT Fanconi anaemia v3.36 RRAS Achchuthan Shanmugasundram Tag gene-checked tag was added to gene: RRAS.
Cytopenia - NOT Fanconi anaemia v3.36 CXCR2 Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: CXCR2.
Tag Q4_23_NHS_review was removed from gene: CXCR2.
Cytopenia - NOT Fanconi anaemia v3.36 RRAS Eleanor Williams Tag Q2_24_promote_green was removed from gene: RRAS.
Cytopenia - NOT Fanconi anaemia v3.36 RRAS Eleanor Williams changed review comment from: The rating of this gene has been updated togreenfollowing NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green following NHS Genomic Medicine Service approval.
Cytopenia - NOT Fanconi anaemia v3.36 RAP1B Eleanor Williams Tag Q4_23_promote_green was removed from gene: RAP1B.
Tag Q4_23_NHS_review was removed from gene: RAP1B.
Cytopenia - NOT Fanconi anaemia v3.36 RAP1B Eleanor Williams changed review comment from: The rating of this gene has been updated togreen and the mode of inheritance set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprintedfollowing NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated to green and the mode of inheritance set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprintedfollowing NHS Genomic Medicine Service approval.
Cytopenia - NOT Fanconi anaemia v3.36 DUT Eleanor Williams Tag Q4_23_promote_green was removed from gene: DUT.
Cytopenia - NOT Fanconi anaemia v3.36 RRAS Eleanor Williams reviewed gene: RRAS: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v3.36 RAP1B Eleanor Williams reviewed gene: RAP1B: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v3.36 DUT Eleanor Williams reviewed gene: DUT: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v3.36 CXCR2 Eleanor Williams reviewed gene: CXCR2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v3.35 RRAS Eleanor Williams Source Expert Review Green was added to RRAS.
Source NHS GMS was added to RRAS.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v3.35 RAP1B Eleanor Williams Source Expert Review Green was added to RAP1B.
Source NHS GMS was added to RAP1B.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v3.35 DUT Eleanor Williams Source Expert Review Green was added to DUT.
Source NHS GMS was added to DUT.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v3.35 CXCR2 Eleanor Williams Source Expert Review Green was added to CXCR2.
Source NHS GMS was added to CXCR2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v3.34 FASLG Dmitrijs Rots gene: FASLG was added
gene: FASLG was added to Cytopenia - NOT Fanconi anaemia. Sources: Other
Mode of inheritance for gene: FASLG was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: FASLG were set to ALPS
Penetrance for gene: FASLG were set to Incomplete
Review for gene: FASLG was set to GREEN
Added comment: FASLG pathogenic variants (germline or somatic) causes ALPS, which has a complex phenotype including different cytopenias (mostly autoimmune).
Sources: Other
Cytopenia - NOT Fanconi anaemia v3.34 CASP10 Dmitrijs Rots gene: CASP10 was added
gene: CASP10 was added to Cytopenia - NOT Fanconi anaemia. Sources: Other
Mode of inheritance for gene: CASP10 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: CASP10 were set to ALPS
Penetrance for gene: CASP10 were set to Incomplete
Review for gene: CASP10 was set to GREEN
Added comment: CASP10 pathogenic variants (germline or somatic) causes ALPS, which has a complex phenotype including different cytopenias (mostly autoimmune).
Sources: Other
Cytopenia - NOT Fanconi anaemia v3.34 FAS Dmitrijs Rots gene: FAS was added
gene: FAS was added to Cytopenia - NOT Fanconi anaemia. Sources: Other
Mode of inheritance for gene: FAS was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: FAS were set to ALPS
Penetrance for gene: FAS were set to Incomplete
Review for gene: FAS was set to GREEN
Added comment: FAS pathogenic variants (germline or somatic) causes ALPS, which has a complex phenotype including different cytopenias (mostly autoimmune).
Sources: Other
Cytopenia - NOT Fanconi anaemia v3.34 RPL27 Hannah Knight reviewed gene: RPL27: Rating: AMBER; Mode of pathogenicity: None; Publications: PMID: 38988374; Phenotypes: ?Diamond-Blackfan anemia 16, 617408; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v3.34 RMRP Sarah Leigh commented on gene: RMRP
Cytopenia - NOT Fanconi anaemia v3.34 RMRP Sarah Leigh Tag locus-type-rna-long-non-coding tag was added to gene: RMRP.
Cytopenia - NOT Fanconi anaemia v3.34 TERC Sarah Leigh Tag locus-type-rna-long-non-coding tag was added to gene: TERC.
Cytopenia - NOT Fanconi anaemia v3.34 RNU4ATAC Sarah Leigh Tag locus-type-rna-small-nuclear tag was added to gene: RNU4ATAC.
Cytopenia - NOT Fanconi anaemia v3.34 LIG4 Arina Puzriakova Phenotypes for gene: LIG4 were changed from 606593 LIG4 syndrome to LIG4 syndrome, OMIM:606593
Cytopenia - NOT Fanconi anaemia v3.33 RNU4ATAC Arina Puzriakova Phenotypes for gene: RNU4ATAC were changed from Roifman syndrome, 616651; Microcephalic osteodysplastic primordial dwarfism, type I, 210710 to Roifman syndrome, OMIM:616651
Cytopenia - NOT Fanconi anaemia v3.32 FCGR3B Arina Puzriakova Classified gene: FCGR3B as Red List (low evidence)
Cytopenia - NOT Fanconi anaemia v3.32 FCGR3B Arina Puzriakova Added comment: Comment on list classification: Demoted from Amber to Red inline with review by Dmitrijs Rots.

Also note review from Helen Brittain (Genomics England Clinical Team) on 100K panel Cytopenias and congenital anaemias (159) from 9 Mar 2017:

"Relevant phenotype affects neutrophils only, on a transient basis owing to presence of antibodies in mother and antigen in fetus (as a result of different genetic factors in father and mother.). Therefore not a germline condition associated with mutations in the child."
Cytopenia - NOT Fanconi anaemia v3.32 FCGR3B Arina Puzriakova Gene: fcgr3b has been classified as Red List (Low Evidence).
Cytopenia - NOT Fanconi anaemia v3.31 RRAS Sarah Leigh Tag Q2_24_promote_green tag was added to gene: RRAS.
Cytopenia - NOT Fanconi anaemia v3.31 RRAS Sarah Leigh Publications for gene: RRAS were set to 34935735
Cytopenia - NOT Fanconi anaemia v3.30 RRAS Sarah Leigh commented on gene: RRAS: RRAS variants have not associated with a phenotype in OMIM or MONDO, but Gen2Phen lists a strong association between RRAS variants and RRAS-related atypical Noonan syndrome. Three germline RRAS variants have been reported (PMID: 24705357; 32815881; 34935735), associated with a RASopathy, which includes myelodysplastic syndrome and contributes to leukaemogenesis.
Cytopenia - NOT Fanconi anaemia v3.30 RRAS Sarah Leigh edited their review of gene: RRAS: Added comment: RRAS variants have not associated with a phenotype in OMIM or MONDO, but Gen2Phen lists a strong association between RRAS variants and RRAS-related atypical Noonan syndrome. Three germline RRAS variants have been reported (PMID: 24705357; 32815881; 34935735), associated with a RASopathy, which includes myelodysplastic syndrome and contributes to leukaemogenesis.; Changed rating: GREEN; Changed publications to: 24705357, 32815881, 34935735; Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Cytopenia - NOT Fanconi anaemia v3.30 RRAS Sarah Leigh Added comment: Comment on phenotypes: RRAS-related atypical Noonan syndrome phenotype from Gen2Phen
Cytopenia - NOT Fanconi anaemia v3.30 RRAS Sarah Leigh Phenotypes for gene: RRAS were changed from Pediatric Myelodysplastic Syndrome to RRAS-related atypical Noonan syndrome
Cytopenia - NOT Fanconi anaemia v3.29 RRAS Sarah Leigh Publications for gene: RRAS were set to PMID: 34935735
Cytopenia - NOT Fanconi anaemia v3.28 RRAS Sarah Leigh Classified gene: RRAS as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v3.28 RRAS Sarah Leigh Gene: rras has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v3.27 CYCS Arina Puzriakova Phenotypes for gene: CYCS were changed from Thrombocytopenia 4, 612004; Thrombocytopenia to Thrombocytopenia 4, OMIM:612004
Cytopenia - NOT Fanconi anaemia v3.26 TUBA4A Achchuthan Shanmugasundram Phenotypes for gene: TUBA4A were changed from Thrombocytopenia to autosomal dominant macrothrombocytopenia, MONDO:0015372
Cytopenia - NOT Fanconi anaemia v3.25 TUBA4A Achchuthan Shanmugasundram Classified gene: TUBA4A as Red List (low evidence)
Cytopenia - NOT Fanconi anaemia v3.25 TUBA4A Achchuthan Shanmugasundram Gene: tuba4a has been classified as Red List (Low Evidence).
Cytopenia - NOT Fanconi anaemia v3.24 TUBA4A Achchuthan Shanmugasundram reviewed gene: TUBA4A: Rating: RED; Mode of pathogenicity: None; Publications: 30760556; Phenotypes: autosomal dominant macrothrombocytopenia, MONDO:0015372; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v3.24 SMARCAL1 Arina Puzriakova Phenotypes for gene: SMARCAL1 were changed from Schimke immunoosseous dysplasia, 242900 to Schimke immunoosseous dysplasia, OMIM:242900
Cytopenia - NOT Fanconi anaemia v3.23 TUBA8 Achchuthan Shanmugasundram edited their review of gene: TUBA8: Changed publications to: 34704371
Cytopenia - NOT Fanconi anaemia v3.23 TUBA8 Achchuthan Shanmugasundram commented on gene: TUBA8: Six unrelated individuals were identified with TUBA8 missense variants in a large cohort of blood donors with mild thrombocytopenia and these individuals were generally asymptomatic and one had menorrhagia. There is also some functional data available.
Cytopenia - NOT Fanconi anaemia v3.23 TUBA8 Achchuthan Shanmugasundram Classified gene: TUBA8 as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v3.23 TUBA8 Achchuthan Shanmugasundram Gene: tuba8 has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v3.22 TUBA8 Achchuthan Shanmugasundram Phenotypes for gene: TUBA8 were changed from Macrothrombocytopenia, isolated, 2, autosomal dominant to Macrothrombocytopenia, isolated, 2, autosomal dominant, OMIM:619840
Cytopenia - NOT Fanconi anaemia v3.21 TUBA8 Achchuthan Shanmugasundram reviewed gene: TUBA8: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Macrothrombocytopenia, isolated, 2, autosomal dominant, OMIM:619840; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v3.21 FCGR3B Dmitrijs Rots reviewed gene: FCGR3B: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
Cytopenia - NOT Fanconi anaemia v3.21 DUT Arina Puzriakova Tag Q4_23_NHS_review was removed from gene: DUT.
Cytopenia - NOT Fanconi anaemia v3.21 DUT Arina Puzriakova Entity copied from Primary immunodeficiency or monogenic inflammatory bowel disease v4.133
Cytopenia - NOT Fanconi anaemia v3.21 DUT Arina Puzriakova gene: DUT was added
gene: DUT was added to Cytopenia - NOT Fanconi anaemia. Sources: Expert Review Amber,Literature
Q4_23_promote_green, Q4_23_NHS_review tags were added to gene: DUT.
Mode of inheritance for gene: DUT was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: DUT were set to 28073829; 35611808; 35931051
Phenotypes for gene: DUT were set to Bone marrow failure and diabetes mellitus syndrome, OMIM:620044
Cytopenia - NOT Fanconi anaemia v3.20 TUBA8 Hannah Knight gene: TUBA8 was added
gene: TUBA8 was added to Cytopenia - NOT Fanconi anaemia. Sources: Literature
Mode of inheritance for gene: TUBA8 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: TUBA8 were set to 34704371
Phenotypes for gene: TUBA8 were set to Macrothrombocytopenia, isolated, 2, autosomal dominant
Review for gene: TUBA8 was set to AMBER
Added comment: PMID: 34704371 (2022) identified rare variants in this gene in patients with macrothrombocytopenia. Associated with a phenotype on OMIM
Sources: Literature
Cytopenia - NOT Fanconi anaemia v3.20 TUBA4A Hannah Knight gene: TUBA4A was added
gene: TUBA4A was added to Cytopenia - NOT Fanconi anaemia. Sources: Literature
Mode of inheritance for gene: TUBA4A was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: TUBA4A were set to 30760556
Phenotypes for gene: TUBA4A were set to Thrombocytopenia
Review for gene: TUBA4A was set to RED
Added comment: Linked to thrombocytopenia (PMID: 30760556, 2019) - only one patient reported
Sources: Literature
Cytopenia - NOT Fanconi anaemia v3.20 SRPRA Achchuthan Shanmugasundram Classified gene: SRPRA as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v3.20 SRPRA Achchuthan Shanmugasundram Added comment: Comment on list classification: As reviewed by Hannah Knight, there is one case and functional studies (including zebrafish model) available in support of the association of this gene with severe congenital neutropenia. Hence, this gene can be rated amber with current evidence.
Cytopenia - NOT Fanconi anaemia v3.20 SRPRA Achchuthan Shanmugasundram Gene: srpra has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v3.19 SRPRA Achchuthan Shanmugasundram Phenotypes for gene: SRPRA were changed from Severe congenital neutropenia to severe congenital neutropenia, MONDO:0018542
Cytopenia - NOT Fanconi anaemia v3.18 SRPRA Achchuthan Shanmugasundram reviewed gene: SRPRA: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: severe congenital neutropenia, MONDO:0018542; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v3.18 SRP19 Achchuthan Shanmugasundram Classified gene: SRP19 as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v3.18 SRP19 Achchuthan Shanmugasundram Added comment: Comment on list classification: As reviewed by Hannah Knight, there are two related families with severe congenital neutropenia and functional studies in support of this association. Hence, this gene can be rated amber with current evidence.
Cytopenia - NOT Fanconi anaemia v3.18 SRP19 Achchuthan Shanmugasundram Gene: srp19 has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v3.17 SRP19 Achchuthan Shanmugasundram Phenotypes for gene: SRP19 were changed from Severe congenital neutropenia to severe congenital neutropenia, MONDO:0018542
Cytopenia - NOT Fanconi anaemia v3.16 SRP19 Achchuthan Shanmugasundram reviewed gene: SRP19: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: severe congenital neutropenia, MONDO:0018542; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v3.16 SEC61A1 Achchuthan Shanmugasundram Publications for gene: SEC61A1 were set to 32325141; 27392076
Cytopenia - NOT Fanconi anaemia v3.15 SEC61A1 Achchuthan Shanmugasundram Phenotypes for gene: SEC61A1 were changed from Severe congenital neutropenia; Tubulointerstitial kidney disease, autosomal dominant, 5 to severe congenital neutropenia, MONDO:0018542; Tubulointerstitial kidney disease, autosomal dominant, 5, OMIM:617056
Cytopenia - NOT Fanconi anaemia v3.14 SEC61A1 Achchuthan Shanmugasundram Classified gene: SEC61A1 as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v3.14 SEC61A1 Achchuthan Shanmugasundram Added comment: Comment on list classification: As reviewed by Hannah Knight, there are two unrelated cases reported with neutropenia. Hence, this gene can be rated amber with the current evidence.
Cytopenia - NOT Fanconi anaemia v3.14 SEC61A1 Achchuthan Shanmugasundram Gene: sec61a1 has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v3.13 SEC61A1 Achchuthan Shanmugasundram reviewed gene: SEC61A1: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: severe congenital neutropenia, MONDO:0018542, Tubulointerstitial kidney disease, autosomal dominant, 5, OMIM:617056; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v3.13 TCIRG1 Achchuthan Shanmugasundram Tag watchlist tag was added to gene: TCIRG1.
Cytopenia - NOT Fanconi anaemia v3.13 TCIRG1 Achchuthan Shanmugasundram Classified gene: TCIRG1 as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v3.13 TCIRG1 Achchuthan Shanmugasundram Added comment: Comment on list classification: Although there are three cases reported so far, only two of these cases were reported in peer-reviewed publications. Hence, this gene is currently rated amber. In addition, watchlist tag has been added.
Cytopenia - NOT Fanconi anaemia v3.13 TCIRG1 Achchuthan Shanmugasundram Gene: tcirg1 has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v3.12 TCIRG1 Achchuthan Shanmugasundram Phenotypes for gene: TCIRG1 were changed from Congenital neutropenia to severe congenital neutropenia, MONDO:0018542
Cytopenia - NOT Fanconi anaemia v3.11 TCIRG1 Achchuthan Shanmugasundram Publications for gene: TCIRG1 were set to 24753205
Cytopenia - NOT Fanconi anaemia v3.10 TCIRG1 Achchuthan Shanmugasundram reviewed gene: TCIRG1: Rating: AMBER; Mode of pathogenicity: None; Publications: 24753205, 35573728; Phenotypes: severe congenital neutropenia, MONDO:0018542; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v3.10 RAP1B Achchuthan Shanmugasundram Tag watchlist was removed from gene: RAP1B.
Tag Q4_23_promote_green tag was added to gene: RAP1B.
Tag Q4_23_NHS_review tag was added to gene: RAP1B.
Cytopenia - NOT Fanconi anaemia v3.10 RAP1B Achchuthan Shanmugasundram Classified gene: RAP1B as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v3.10 RAP1B Achchuthan Shanmugasundram Added comment: Comment on list classification: There are three unrelated cases with cytopenia and hence this gene can be promoted to green rating in the next GMS review.

This gene has been associated with relevant phenotype in Gene2Phenotype database (with 'limited' rating in the DD panel), but not yet been associated with phenotypes in OMIM.
Cytopenia - NOT Fanconi anaemia v3.10 RAP1B Achchuthan Shanmugasundram Gene: rap1b has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v3.9 RAP1B Achchuthan Shanmugasundram Publications for gene: RAP1B were set to 32627184; 26280580
Cytopenia - NOT Fanconi anaemia v3.8 RAP1B Achchuthan Shanmugasundram Mode of inheritance for gene: RAP1B was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v3.7 RAP1B Achchuthan Shanmugasundram reviewed gene: RAP1B: Rating: GREEN; Mode of pathogenicity: None; Publications: 32627184, 35451551; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v3.4 CXCR2 Achchuthan Shanmugasundram Tag Q4_23_NHS_review tag was added to gene: CXCR2.
Cytopenia - NOT Fanconi anaemia v3.4 SRP19 Hannah Knight gene: SRP19 was added
gene: SRP19 was added to Cytopenia - NOT Fanconi anaemia. Sources: Literature
Mode of inheritance for gene: SRP19 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: SRP19 were set to 36223592
Phenotypes for gene: SRP19 were set to Severe congenital neutropenia
Review for gene: SRP19 was set to AMBER
Added comment: PMID: 36223592 - a novel homozygous variant in SRP19 was identified in 2 related pedigrees with 5 patients affected (c.189+5G>A) + functional studies
Sources: Literature
Cytopenia - NOT Fanconi anaemia v3.4 SRPRA Hannah Knight gene: SRPRA was added
gene: SRPRA was added to Cytopenia - NOT Fanconi anaemia. Sources: Literature
Mode of inheritance for gene: SRPRA was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: SRPRA were set to 36223592
Phenotypes for gene: SRPRA were set to Severe congenital neutropenia
Review for gene: SRPRA was set to AMBER
Added comment: PMID: 36223592 - A novel heterozygous de novo variant in SRPRA was found in 1 pedigree with 1 patient (p.Gln464Glu) - results in an amino acid exchange (glutamine to glutamic acid, position 464) in an alpha helix loop close to the GTPase active center known to mediate interaction with the cognate-binding partner, SRP54 (known cause of SCN)
+ functional studies
Sources: Literature
Cytopenia - NOT Fanconi anaemia v3.4 SEC61A1 Hannah Knight gene: SEC61A1 was added
gene: SEC61A1 was added to Cytopenia - NOT Fanconi anaemia. Sources: Literature
Mode of inheritance for gene: SEC61A1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: SEC61A1 were set to 32325141; 27392076
Phenotypes for gene: SEC61A1 were set to Severe congenital neutropenia; Tubulointerstitial kidney disease, autosomal dominant, 5
Review for gene: SEC61A1 was set to AMBER
Added comment: PMID: 32325141 - reported a patient with a de novo variant in this gene, presenting with severe congenital neutropenia and recurrent infections
PMID: 27392076 - neutropenia previously reported in a father and daughter with tubulointerstitial kidney disease due to a heterozygous SEC61A1 variant
Sources: Literature
Cytopenia - NOT Fanconi anaemia v3.4 CXCR2 Achchuthan Shanmugasundram Phenotypes for gene: CXCR2 were changed from ?WHIM syndrome 2 to ?WHIM syndrome 2, OMIM:619407
Cytopenia - NOT Fanconi anaemia v3.3 CXCR2 Achchuthan Shanmugasundram Classified gene: CXCR2 as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v3.3 CXCR2 Achchuthan Shanmugasundram Added comment: Comment on list classification: As reviewed by Hannah Knight, there are five unrelated cases available in support of the association of biallelic CXCR2 variants to this panel. Hence, this gene can be promoted to green rating in the next GMS review.
Cytopenia - NOT Fanconi anaemia v3.3 CXCR2 Achchuthan Shanmugasundram Gene: cxcr2 has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v3.2 CXCR2 Achchuthan Shanmugasundram Tag Q4_23_promote_green tag was added to gene: CXCR2.
Cytopenia - NOT Fanconi anaemia v3.2 CXCR2 Achchuthan Shanmugasundram reviewed gene: CXCR2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ?WHIM syndrome 2, OMIM:619407; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v3.2 CXCR2 Hannah Knight gene: CXCR2 was added
gene: CXCR2 was added to Cytopenia - NOT Fanconi anaemia. Sources: Literature
Mode of inheritance for gene: CXCR2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: CXCR2 were set to 24777453; 34854278
Phenotypes for gene: CXCR2 were set to ?WHIM syndrome 2
Review for gene: CXCR2 was set to GREEN
Added comment: Five patients reported with biallelic variants. 2 sisters with neutropaenia, myelokathexis, and recurrent bacterial infections and homozygous frameshift variant in this gene (PMID: 24777453). Of other four patients, one had biallelic null variants and presented with neutropenia and myelokathexis (PMID: 34854278). Others all had biallelic missense variants, and presented with neutropenia
Sources: Literature
Cytopenia - NOT Fanconi anaemia v3.2 RAP1B Hannah Knight reviewed gene: RAP1B: Rating: GREEN; Mode of pathogenicity: None; Publications: 35451551; Phenotypes: Syndromic thrombocytopenia; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Cytopenia - NOT Fanconi anaemia v3.2 TCIRG1 Hannah Knight gene: TCIRG1 was added
gene: TCIRG1 was added to Cytopenia - NOT Fanconi anaemia. Sources: Literature
Mode of inheritance for gene: TCIRG1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: TCIRG1 were set to 24753205
Phenotypes for gene: TCIRG1 were set to Congenital neutropenia
Penetrance for gene: TCIRG1 were set to unknown
Review for gene: TCIRG1 was set to AMBER
Added comment: A specific, novel variant in TCIRG1 (R736S) identified as the probable cause for SCN in a large multigenerational family through exome sequencing (Makaryan et al. 2014 - PMID 24753205)
In 2022, a new family identified in Taiwan to have a variant affecting the same amino acid (R736C) - https://doi.org/10.1182/blood-2022-159214
Sources: Literature
Cytopenia - NOT Fanconi anaemia v3.2 MECOM Arina Puzriakova Phenotypes for gene: MECOM were changed from Radioulnar synostosis with amegakaryocytic thrombocytopenia 2, 616738; 616738 Radioulnar synostosis with amegakaryocytic thrombocytopenia 2 to Radioulnar synostosis with amegakaryocytic thrombocytopenia 2, OMIM:616738
Cytopenia - NOT Fanconi anaemia v3.1 Catherine Snow Panel version 3.0 has been signed off on 2023-03-22
Cytopenia - NOT Fanconi anaemia v3.0 Catherine Snow promoted panel to version 3.0
Cytopenia - NOT Fanconi anaemia v2.4 RPL27 Achchuthan Shanmugasundram changed review comment from: The rating of this gene has been updated to Amber following NHS Genomic Medicine Service approval. The GMS reviewers note that this gene should be demoted to amber as there is only one case, but supported by functional studies and mutation of multiple other ribosomal genes results in the same phenotype.; to: The rating of this gene has been updated to Amber following NHS Genomic Medicine Service approval. The GMS reviewers note that this gene should be demoted to amber as there is only one case, but supported by functional studies and mutation of multiple other ribosomal genes results in the same phenotype.
Cytopenia - NOT Fanconi anaemia v2.4 RPL27 Achchuthan Shanmugasundram reviewed gene: RPL27: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
Cytopenia - NOT Fanconi anaemia v2.4 RPL27 Achchuthan Shanmugasundram Deleted their review
Cytopenia - NOT Fanconi anaemia v2.4 RPL27 Achchuthan Shanmugasundram Deleted their comment
Cytopenia - NOT Fanconi anaemia v2.4 RPL27 Achchuthan Shanmugasundram Classified gene: RPL27 as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v2.4 RPL27 Achchuthan Shanmugasundram Gene: rpl27 has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v2.3 RPL27 Achchuthan Shanmugasundram Tag Q3_22_rating was removed from gene: RPL27.
Tag Q3_22_expert_review was removed from gene: RPL27.
Cytopenia - NOT Fanconi anaemia v2.3 GP1BB Achchuthan Shanmugasundram changed review comment from: After NHS Genomic Medicine Service consideration, the rating of this gene has not been changed and remains Amber.; to: After NHS Genomic Medicine Service consideration, the rating of this gene has not been changed and remains Amber. GMS reviewers also note that mutations are associated with only platelet features not multi-lineage cytopenias.
Cytopenia - NOT Fanconi anaemia v2.3 GP1BB Achchuthan Shanmugasundram Tag Q2_22_rating was removed from gene: GP1BB.
Cytopenia - NOT Fanconi anaemia v2.3 RPA1 Achchuthan Shanmugasundram Tag Q2_22_rating was removed from gene: RPA1.
Cytopenia - NOT Fanconi anaemia v2.3 MPL Achchuthan Shanmugasundram changed review comment from: The mode of inheritance of this gene has been updated to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval.; to: The mode of inheritance of this gene has been updated to 'BIALLELIC, autosomal or pseudoautosomal' following NHS Genomic Medicine Service approval. GMS reviewers also note that the monoallelic variants that were previously reported for this gene were associated with thrombocythaemia and not with thrombocytopenia.
Cytopenia - NOT Fanconi anaemia v2.3 MPL Achchuthan Shanmugasundram Tag Q2_22_MOI was removed from gene: MPL.
Tag Q2_22_expert_review was removed from gene: MPL.
Cytopenia - NOT Fanconi anaemia v2.3 KLF1 Achchuthan Shanmugasundram Tag Q1_22_MOI was removed from gene: KLF1.
Cytopenia - NOT Fanconi anaemia v2.3 CLPB Achchuthan Shanmugasundram Tag Q4_21_rating was removed from gene: CLPB.
Cytopenia - NOT Fanconi anaemia v2.3 RPL27 Achchuthan Shanmugasundram reviewed gene: RPL27: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v2.3 GP1BB Achchuthan Shanmugasundram reviewed gene: GP1BB: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v2.3 RPA1 Achchuthan Shanmugasundram reviewed gene: RPA1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v2.3 MPL Achchuthan Shanmugasundram commented on gene: MPL
Cytopenia - NOT Fanconi anaemia v2.3 KLF1 Achchuthan Shanmugasundram commented on gene: KLF1
Cytopenia - NOT Fanconi anaemia v2.3 CLPB Achchuthan Shanmugasundram reviewed gene: CLPB: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v2.2 RPA1 Achchuthan Shanmugasundram Source Expert Review Green was added to RPA1.
Source NHS GMS was added to RPA1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v2.2 MPL Achchuthan Shanmugasundram Mode of inheritance for gene MPL was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v2.2 KLF1 Achchuthan Shanmugasundram Mode of inheritance for gene KLF1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v2.2 CLPB Achchuthan Shanmugasundram Source Expert Review Green was added to CLPB.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v2.1 RRAS Dmitrijs Rots gene: RRAS was added
gene: RRAS was added to Cytopenia - NOT Fanconi anaemia. Sources: Literature
Mode of inheritance for gene: RRAS was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: RRAS were set to PMID: 34935735
Phenotypes for gene: RRAS were set to Pediatric Myelodysplastic Syndrome
Penetrance for gene: RRAS were set to unknown
Mode of pathogenicity for gene: RRAS was set to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments
Review for gene: RRAS was set to GREEN
Added comment: 34935735 describes a new case and provides info from 3 cases from the literature with RASopathy AND pediatric MDS. Only de novo missense variants were found. Therefore, enough evidence for green rating.
Sources: Literature
Cytopenia - NOT Fanconi anaemia v2.1 Catherine Snow Panel version 2.0 has been signed off on 2022-11-30
Cytopenia - NOT Fanconi anaemia v2.0 Catherine Snow promoted panel to version 2.0
Cytopenia - NOT Fanconi anaemia v1.73 TERT Arina Puzriakova Phenotypes for gene: TERT were changed from {Pulmonary fibrosis, telomere-related, 1}, 614742; {Dyskeratosis congenita, autosomal dominant 2}, 613989; Coronary artery disease; {Melanoma, cutaneous malignant, 9}, 615134; 614742 Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1; Aplastic Anemia; 614742 {Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1}; {Leukemia, acute myeloid}, 601626; 613989 Dyskeratosis congenita; {Dyskeratosis congenita, autosomal recessive 4}, 613989 to Dyskeratosis congenita, autosomal dominant 2, OMIM:613989; Dyskeratosis congenita, autosomal recessive 4, OMIM:613989; Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1, OMIM:614742
Cytopenia - NOT Fanconi anaemia v1.72 RPL27 Eleanor Williams commented on gene: RPL27
Cytopenia - NOT Fanconi anaemia v1.72 RPL27 Eleanor Williams Tag Q2_21_expert_review was removed from gene: RPL27.
Tag Q3_22_rating tag was added to gene: RPL27.
Tag Q3_22_expert_review tag was added to gene: RPL27.
Cytopenia - NOT Fanconi anaemia v1.72 CLPB Arina Puzriakova Phenotypes for gene: CLPB were changed from 3-methylglutaconic aciduria, type VII, with cataracts, neurologic involvement and neutropenia, OMIM:616271 to 3-methylglutaconic aciduria, type VIIB, autosomal recessive, OMIM:616271; 3-methylglutaconic aciduria, type VIIA, autosomal dominant, OMIM:619835; Neutropenia, severe congenital, 9, autosomal dominant, OMIM:619813
Cytopenia - NOT Fanconi anaemia v1.71 CLPB Arina Puzriakova Publications for gene: CLPB were set to 25597510; 25597511; 25650066; 26916670; 28687938; 34140661
Cytopenia - NOT Fanconi anaemia v1.70 SLC37A4 Arina Puzriakova Phenotypes for gene: SLC37A4 were changed from Glycogen storage disease Ib, 232220 to Glycogen storage disease Ib, OMIM:232220; Glycogen storage disease Ic, OMIM:232240
Cytopenia - NOT Fanconi anaemia v1.69 CLPB Dmitrijs Rots edited their review of gene: CLPB: Added comment: additional evidence in PMID: 34115842; Changed publications to: PMID: 34140661, 34115842
Cytopenia - NOT Fanconi anaemia v1.69 TAZ Arina Puzriakova commented on gene: TAZ
Cytopenia - NOT Fanconi anaemia v1.69 TAZ Arina Puzriakova Tag new-gene-name tag was added to gene: TAZ.
Cytopenia - NOT Fanconi anaemia v1.69 GP1BB Arina Puzriakova Publications for gene: GP1BB were set to
Cytopenia - NOT Fanconi anaemia v1.68 GP1BB Arina Puzriakova Classified gene: GP1BB as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v1.68 GP1BB Arina Puzriakova Added comment: Comment on list classification: This gene should be promoted to Green at the next GMS review. Variants are associated with Bernard-Soulier syndrome characterised by thrombocytopenia (within the scope of this panel), giant platelets and bleeding tendency. Sufficient cases for both inheritance patterns to rate as green with an AD/AR mode of inheritance.
Cytopenia - NOT Fanconi anaemia v1.68 GP1BB Arina Puzriakova Gene: gp1bb has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v1.67 GP1BB Arina Puzriakova Tag Q2_22_rating tag was added to gene: GP1BB.
Cytopenia - NOT Fanconi anaemia v1.67 GP1BB Arina Puzriakova Mode of inheritance for gene: GP1BB was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v1.66 GP1BB Arina Puzriakova Added comment: Comment on mode of inheritance: Updated from 'biallelic' to 'both mono- and biallelic' to align with the MOI set on other panels (Inherited bleeding disorders, Bleeding and platelet disorders). PMID:28064200 provides evidence for AD inheritance of macrothrombocytopenia.
Cytopenia - NOT Fanconi anaemia v1.66 GP1BB Arina Puzriakova Mode of inheritance for gene: GP1BB was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v1.65 GP1BB Arina Puzriakova Phenotypes for gene: GP1BB were changed from Bernard-Soulier syndrome, type B, 231200; Mild macrothrombocytopenia to Bernard-Soulier syndrome, type B, OMIM:231200; Giant platelet disorder, isolated, OMIM:231200; Macrothrombocytopenia
Cytopenia - NOT Fanconi anaemia v1.64 PARN Arina Puzriakova Phenotypes for gene: PARN were changed from 616371 Pulmonary fibrosis and/or bone marrow failure, telomere-related, 4; 616353 Dyskeratosis congenita, autosomal recessive 6; 616353 Dyskeratosis congenita, autosomal recessive 6 to Dyskeratosis congenita, autosomal recessive 6, OMIM:616353; Pulmonary fibrosis and/or bone marrow failure, telomere-related, 4, OMIM:616371
Cytopenia - NOT Fanconi anaemia v1.63 MPL Arina Puzriakova Added comment: Comment on mode of inheritance: The MOI on this panel should be reviewed at the next GMS panel update to determine the pertinent inheritance pattern (currently set to both AD/AR).

Biallelic variants cause thrombocytopenia (MIM# 604498) which in severe forms can present with pancytopenia, a phenotype that is within the scope of this panel. On the other hand, monoallelic variants are associated with thrombocythemia (MIM# 601977) which does not include features that may be relevant here. Therefore it may be appropriate to update the MOI to 'biallelic' only.
Cytopenia - NOT Fanconi anaemia v1.63 MPL Arina Puzriakova Mode of inheritance for gene: MPL was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v1.62 MPL Arina Puzriakova Tag Q2_22_MOI tag was added to gene: MPL.
Tag Q2_22_expert_review tag was added to gene: MPL.
Cytopenia - NOT Fanconi anaemia v1.62 MPL Arina Puzriakova Phenotypes for gene: MPL were changed from 601977 Thrombocythemia 2; 604498 Thrombocytopenia, congenital amegakaryocytic; Thrombocytopenia, congenital amegakaryocytic, 604498 to Thrombocytopenia, congenital amegakaryocytic, OMIM:604498
Cytopenia - NOT Fanconi anaemia v1.61 RPA1 Arina Puzriakova Classified gene: RPA1 as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v1.61 RPA1 Arina Puzriakova Added comment: Comment on list classification: Despite the heterogenous phenotypes observed, there are sufficient cases (3) with hematopoietic manifestations to warrant a green rating on this panel at the next GMS review.
Cytopenia - NOT Fanconi anaemia v1.61 RPA1 Arina Puzriakova Gene: rpa1 has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v1.60 RPA1 Arina Puzriakova Tag Q2_22_rating tag was added to gene: RPA1.
Cytopenia - NOT Fanconi anaemia v1.60 RPA1 Arina Puzriakova Penetrance for gene RPA1 was set from to unknown
Cytopenia - NOT Fanconi anaemia v1.59 RPA1 Arina Puzriakova Publications for gene: RPA1 were set to
Cytopenia - NOT Fanconi anaemia v1.58 RPA1 Arina Puzriakova reviewed gene: RPA1: Rating: GREEN; Mode of pathogenicity: None; Publications: 34767620; Phenotypes: Pulmonary fibrosis and/or bone marrow failure, telomere-related, 6, OMIM:619767; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v1.58 RPA1 Arina Puzriakova Phenotypes for gene: RPA1 were changed from bone marrow failure; T- and B-cell lymphopenia; pulmonary fibrosis; skin manifestations. to Pulmonary fibrosis and/or bone marrow failure, telomere-related, 6, OMIM:619767
Cytopenia - NOT Fanconi anaemia v1.57 RPL31 Arina Puzriakova Tag for-review was removed from gene: RPL31.
Cytopenia - NOT Fanconi anaemia v1.57 RPL31 Arina Puzriakova changed review comment from: The rating of this gene has been updated following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated following NHS Genomic Medicine Service approval. It has been agreed that RPL31 should be amber.
Cytopenia - NOT Fanconi anaemia v1.57 RPL9 Arina Puzriakova Tag for-review was removed from gene: RPL9.
Cytopenia - NOT Fanconi anaemia v1.57 KIF23 Arina Puzriakova Tag for-review was removed from gene: KIF23.
Cytopenia - NOT Fanconi anaemia v1.57 RPL26 Arina Puzriakova Tag for-review was removed from gene: RPL26.
Cytopenia - NOT Fanconi anaemia v1.57 KIF23 Arina Puzriakova changed review comment from: The rating of this gene has been updated following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated following NHS Genomic Medicine Service approval. It has been agreed that KIF23 should be amber.
Cytopenia - NOT Fanconi anaemia v1.57 RPL9 Arina Puzriakova changed review comment from: The rating of this gene has been updated following NHS Genomic Medicine Service approval.; to: The rating of this gene has been updated following NHS Genomic Medicine Service approval. It has been agreed that RPL9 should be amber.
Cytopenia - NOT Fanconi anaemia v1.57 STN1 Arina Puzriakova Tag for-review was removed from gene: STN1.
Cytopenia - NOT Fanconi anaemia v1.57 SRP54 Arina Puzriakova Tag for-review was removed from gene: SRP54.
Cytopenia - NOT Fanconi anaemia v1.57 AK2 Arina Puzriakova Tag for-review was removed from gene: AK2.
Cytopenia - NOT Fanconi anaemia v1.57 DDX41 Arina Puzriakova Tag for-review was removed from gene: DDX41.
Cytopenia - NOT Fanconi anaemia v1.57 NHP2 Arina Puzriakova Tag for-review was removed from gene: NHP2.
Cytopenia - NOT Fanconi anaemia v1.57 MYSM1 Arina Puzriakova Tag for-review was removed from gene: MYSM1.
Cytopenia - NOT Fanconi anaemia v1.57 EFL1 Arina Puzriakova Tag for-review was removed from gene: EFL1.
Cytopenia - NOT Fanconi anaemia v1.57 RPL31 Arina Puzriakova commented on gene: RPL31: The rating of this gene has been updated following NHS Genomic Medicine Service approval.
Cytopenia - NOT Fanconi anaemia v1.57 RPL26 Arina Puzriakova commented on gene: RPL26: The rating of this gene has been updated following NHS Genomic Medicine Service approval.
Cytopenia - NOT Fanconi anaemia v1.57 KIF23 Arina Puzriakova commented on gene: KIF23: The rating of this gene has been updated following NHS Genomic Medicine Service approval.
Cytopenia - NOT Fanconi anaemia v1.57 RPL9 Arina Puzriakova commented on gene: RPL9: The rating of this gene has been updated following NHS Genomic Medicine Service approval.
Cytopenia - NOT Fanconi anaemia v1.57 STN1 Arina Puzriakova commented on gene: STN1
Cytopenia - NOT Fanconi anaemia v1.57 SRP54 Arina Puzriakova commented on gene: SRP54: The rating of this gene has been updated following NHS Genomic Medicine Service approval.
Cytopenia - NOT Fanconi anaemia v1.57 AK2 Arina Puzriakova commented on gene: AK2: The rating of this gene has been updated following NHS Genomic Medicine Service approval.
Cytopenia - NOT Fanconi anaemia v1.57 DDX41 Arina Puzriakova commented on gene: DDX41: The rating of this gene has been updated following NHS Genomic Medicine Service approval.
Cytopenia - NOT Fanconi anaemia v1.57 NHP2 Arina Puzriakova commented on gene: NHP2: The rating of this gene has been updated following NHS Genomic Medicine Service approval.
Cytopenia - NOT Fanconi anaemia v1.57 MYSM1 Arina Puzriakova commented on gene: MYSM1: The rating of this gene has been updated following NHS Genomic Medicine Service approval.
Cytopenia - NOT Fanconi anaemia v1.57 EFL1 Arina Puzriakova commented on gene: EFL1
Cytopenia - NOT Fanconi anaemia v1.56 RPL31 Arina Puzriakova Source Expert Review Amber was added to RPL31.
Rating Changed from Green List (high evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v1.56 RPL26 Arina Puzriakova Source Expert Review Red was added to RPL26.
Rating Changed from Green List (high evidence) to Red List (low evidence)
Cytopenia - NOT Fanconi anaemia v1.56 KIF23 Arina Puzriakova Source Expert Review Amber was added to KIF23.
Rating Changed from Green List (high evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v1.56 RPL9 Arina Puzriakova Source Expert Review Amber was added to RPL9.
Rating Changed from Green List (high evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v1.56 STN1 Arina Puzriakova Source Expert Review Green was added to STN1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v1.56 SRP54 Arina Puzriakova Source Expert Review Green was added to SRP54.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v1.56 AK2 Arina Puzriakova Source Expert Review Green was added to AK2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v1.56 DDX41 Arina Puzriakova Source Expert Review Green was added to DDX41.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v1.56 NHP2 Arina Puzriakova Source Expert Review Green was added to NHP2.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v1.56 MYSM1 Arina Puzriakova Source Expert Review Green was added to MYSM1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v1.56 EFL1 Arina Puzriakova Source Expert Review Green was added to EFL1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v1.55 KLF1 Arina Puzriakova Tag Q1_22_MOI tag was added to gene: KLF1.
Cytopenia - NOT Fanconi anaemia v1.55 KLF1 Arina Puzriakova Added comment: Comment on mode of inheritance: MOI should be updated from 'Monoallelic' only to 'Both mono- and biallelic, (biallelic more severe)'.

The expanded MOI is based on compound heterozygous cases in PMID:24443441; 25724378; 27282573; 28361594; 28369821. Heterozygous carrier parents may display features of beta thalassemia.
Cytopenia - NOT Fanconi anaemia v1.55 KLF1 Arina Puzriakova Mode of inheritance for gene: KLF1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Cytopenia - NOT Fanconi anaemia v1.54 KLF1 Arina Puzriakova Publications for gene: KLF1 were set to 21055716
Cytopenia - NOT Fanconi anaemia v1.53 KLF1 Arina Puzriakova Phenotypes for gene: KLF1 were changed from Dyserythropoietic anemia, congenital, type IV, 613673; Congenital Dyserythropoietic Anemia to Dyserythropoietic anemia, congenital, type IV, OMIM:613673
Cytopenia - NOT Fanconi anaemia v1.52 ADA2 Arina Puzriakova Phenotypes for gene: ADA2 were changed from Diamond Blackfan anaemia; 615688 Polyarteritis nodosa/Sneddon sydrome to Vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome, OMIM:615688; Sneddon syndrome, OMIM:182410; Diamond-Blackfan Anemia
Cytopenia - NOT Fanconi anaemia v1.51 PSMB8 Arina Puzriakova Phenotypes for gene: PSMB8 were changed from Proteasome-associated autoinflammatory syndrome 1 and digenic forms, 256040 to Proteasome-associated autoinflammatory syndrome 1 and digenic forms, OMIM:256040
Cytopenia - NOT Fanconi anaemia v1.50 POLR2C Ivone Leong Phenotypes for gene: POLR2C were changed from Primary ovarian insufficiency to thrombocytopenia, MONDO:0002049
Cytopenia - NOT Fanconi anaemia v1.49 POLR2C Ivone Leong Classified gene: POLR2C as Red List (low evidence)
Cytopenia - NOT Fanconi anaemia v1.49 POLR2C Ivone Leong Gene: polr2c has been classified as Red List (Low Evidence).
Cytopenia - NOT Fanconi anaemia v1.48 POLR2C Ivone Leong changed review comment from: Comment on list classification: New gene added by Zornitza Stark (Australian Genomics). This gene is not associated with a phenotype in OMIM or Gene2Phenotype. The affected patients in PMID: 29367954 also had hypothyroidism (3/5), thrombocytopenia (2/5) and pernicious anaemia (2/5).; to: Comment on list classification: New gene added by Zornitza Stark (Australian Genomics). This gene is not associated with a phenotype in OMIM or Gene2Phenotype. The affected patients in PMID: 29367954 also had hypothyroidism (3/5), thrombocytopenia (2/5) and pernicious anaemia (2/5). The entries in ClinVar did not mention any other phenotype. So therefore this gene has been given a Red rating.
Cytopenia - NOT Fanconi anaemia v1.48 POLR2C Ivone Leong Tag watchlist was removed from gene: POLR2C.
Cytopenia - NOT Fanconi anaemia v1.48 POLR2C Ivone Leong Entity copied from Primary ovarian insufficiency v1.62
Cytopenia - NOT Fanconi anaemia v1.48 POLR2C Ivone Leong gene: POLR2C was added
gene: POLR2C was added to Cytopenia - NOT Fanconi anaemia. Sources: Expert Review Amber,Literature
watchlist tags were added to gene: POLR2C.
Mode of inheritance for gene: POLR2C was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: POLR2C were set to 34794894; 29367954
Phenotypes for gene: POLR2C were set to Primary ovarian insufficiency
Cytopenia - NOT Fanconi anaemia v1.47 CLPB Arina Puzriakova Tag Q4_21_rating tag was added to gene: CLPB.
Cytopenia - NOT Fanconi anaemia v1.47 CLPB Arina Puzriakova Classified gene: CLPB as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v1.47 CLPB Arina Puzriakova Added comment: Comment on list classification: Upgraded from Red to Amber but should be made Green at the next GMS panel update.

Neutropenia is often reported and can be a severe and early feature, sometimes present from birth. Neutropenia was observed in at least 11 biallelic cases and 5 monoallelic cases which is sufficient for a Green rating under the MOI 'Both mono- and biallelic'
Cytopenia - NOT Fanconi anaemia v1.47 CLPB Arina Puzriakova Gene: clpb has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v1.46 CLPB Arina Puzriakova Publications for gene: CLPB were set to
Cytopenia - NOT Fanconi anaemia v1.45 CLPB Arina Puzriakova Mode of inheritance for gene: CLPB was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v1.44 CLPB Arina Puzriakova Phenotypes for gene: CLPB were changed from 3-methylglutaconic aciduria, type VII, with cataracts, neurologic involvement and neutropenia, 616271 to 3-methylglutaconic aciduria, type VII, with cataracts, neurologic involvement and neutropenia, OMIM:616271
Cytopenia - NOT Fanconi anaemia v1.43 RPA1 Dmitrijs Rots gene: RPA1 was added
gene: RPA1 was added to Cytopenia - NOT Fanconi anaemia. Sources: Literature
Mode of inheritance for gene: RPA1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: RPA1 were set to bone marrow failure; T- and B-cell lymphopenia; pulmonary fibrosis; skin manifestations.
Penetrance for gene: RPA1 were set to unknown
Mode of pathogenicity for gene: RPA1 was set to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments
Review for gene: RPA1 was set to GREEN
Added comment: 4 cases with gain of function mutations with "including bone marrow failure, myelodysplastic syndrome, T- and B-cell lymphopenia, pulmonary fibrosis, or skin manifestations." described in
https://doi.org/10.1182/blood.2021011980
Sources: Literature
Cytopenia - NOT Fanconi anaemia v1.43 CLPB Dmitrijs Rots reviewed gene: CLPB: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 34140661; Phenotypes: Neutropenia, intellectual disability; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v1.43 RPS27 Arina Puzriakova Phenotypes for gene: RPS27 were changed from Diamond-Blackfan anemia; ?Diamond-Blackfan anemia 17, 617409 to ?Diamond-Blackfan anemia 17, OMIM:617409
Cytopenia - NOT Fanconi anaemia v1.42 FLNA Arina Puzriakova Mode of inheritance for gene: FLNA was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Cytopenia - NOT Fanconi anaemia v1.41 FLNA Arina Puzriakova Phenotypes for gene: FLNA were changed from to Heterotopia, periventricular, 1, OMIM:300049; Macrothrombocytopenia
Cytopenia - NOT Fanconi anaemia v1.40 ACD Ivone Leong Added comment: Comment on mode of inheritance: MOI changed from "BOTH monoallelic and biallelic, autosomal or pseudoautosomal" to "BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal" as the patient with AR inheritance had a more severe phenotype.
Cytopenia - NOT Fanconi anaemia v1.40 ACD Ivone Leong Mode of inheritance for gene: ACD was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v1.39 ACD Arina Puzriakova Phenotypes for gene: ACD were changed from 616553 ?Dyskeratosis congenita 6 and 7 to Dyskeratosis congenita, autosomal dominant 6, OMIM:616553; Dyskeratosis congenita, autosomal recessive 7, OMIM:616553
Cytopenia - NOT Fanconi anaemia v1.38 ACD Arina Puzriakova Classified gene: ACD as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v1.38 ACD Arina Puzriakova Added comment: Comment on list classification: Only two families with DC who have variants in ACD have been reported since 2015 - one family with AD inheritance had only progressive bone marrow failure (PMID: 25205116) and one patient (patient B) with AR inheritance had a more severe phenotype (PMID: 25233904). However, this gene was rated Green on this and other panels following external clinical review - so this rating will be maintained at this time.
Cytopenia - NOT Fanconi anaemia v1.38 ACD Arina Puzriakova Gene: acd has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v1.37 ACD Zornitza Stark reviewed gene: ACD: Rating: RED; Mode of pathogenicity: None; Publications: 25205116, 25233904; Phenotypes: Dyskeratosis congenita, MIM# 616553; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v1.37 ARPC1B Arina Puzriakova Phenotypes for gene: ARPC1B were changed from Platelet abnormalities with eosinophilia and immune-mediated inflammatory disease, 617718 to Immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia, OMIM:617718
Cytopenia - NOT Fanconi anaemia v1.36 RPL27 Arina Puzriakova commented on gene: RPL27
Cytopenia - NOT Fanconi anaemia v1.36 RPL27 Arina Puzriakova Tag Q2_21_expert_review tag was added to gene: RPL27.
Cytopenia - NOT Fanconi anaemia v1.36 ADAMTS13 Arina Puzriakova Phenotypes for gene: ADAMTS13 were changed from Thrombotic thrombocytopenic purpura, familial, 274150 to Thrombotic thrombocytopenic purpura, hereditary, OMIM:274150
Cytopenia - NOT Fanconi anaemia v1.35 RPL27 Zornitza Stark reviewed gene: RPL27: Rating: RED; Mode of pathogenicity: None; Publications: 25424902; Phenotypes: Diamond-Blackfan anemia 16, MIM# 617408; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v1.35 RPL31 Arina Puzriakova Classified gene: RPL31 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v1.35 RPL31 Arina Puzriakova Added comment: Comment on list classification: Current Green gene rating based on GMS specialist test group consensus. However, note the recent review by Zornitza Stark (Australian Genomics) highlighting limited published evidence to support this gene-disease association, which is only sufficient for an Amber rating at present. Will be flagged for review at the next GMS panel update (added 'for-review' tag).
Cytopenia - NOT Fanconi anaemia v1.35 RPL31 Arina Puzriakova Gene: rpl31 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v1.34 RPL31 Arina Puzriakova Tag for-review tag was added to gene: RPL31.
Cytopenia - NOT Fanconi anaemia v1.34 RAP1B Ivone Leong Classified gene: RAP1B as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v1.34 RAP1B Ivone Leong Gene: rap1b has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v1.33 RAP1B Ivone Leong gene: RAP1B was added
gene: RAP1B was added to Cytopenia - NOT Fanconi anaemia. Sources: Literature
watchlist tags were added to gene: RAP1B.
Mode of inheritance for gene: RAP1B was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Publications for gene: RAP1B were set to 32627184; 26280580
Phenotypes for gene: RAP1B were set to Syndromic intellectual disability; cytopenia
Review for gene: RAP1B was set to AMBER
Added comment: This gene is associated with a phenotype in Gene2Phenotype but not OMIM.

PMID: 32627184 describes 2 patients.
36 yo patient of non-consanguineous parents. Had unclear pancytopenia, multiple congenital malformations, mild intellectual disability, endocrine disorders (short stature with growth hormone deficiency), dysmorphism and other features. Parents and sibling unaffected.
13 yo of non-consanguineous parents with thrombocytopenia, multiple congenital anomalies and learning difficulties. He had normal developmental milestones, walk was achieved at 14 months and there was no speech delay. He attended mainstream school with auxiliary help because of learning difficulties with graphism, syntaxic comprehension, logical reasoning and attention deficit. Parents and siblings unaffected.

PMID: 26280580 describes another patient with variant in RAP1B. The clinical features can be found in supplementary table 2. The table lists ID, but doesn't say severity and lists a host of other features including short stature, facial dysmorphism and skeletal findings. Cytopenia is not a feature for this patient.

All 3 cases seem to have a very wide spectrum of differing phenotypes and therefore, this gene has been given an Amber rating until further evidence is available.
Sources: Literature
Cytopenia - NOT Fanconi anaemia v1.32 STN1 Sarah Leigh Classified gene: STN1 as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v1.32 STN1 Sarah Leigh Added comment: Comment on list classification: Associated with relevant phenotype in OMIM and as probable Gen2Phen gene. At least four variants reported in three unrelated cases, together with a supportive zebrafish model and other functional studies.

There is enough evidence for this gene to be rated GREEN at the next major review.
Cytopenia - NOT Fanconi anaemia v1.32 STN1 Sarah Leigh Gene: stn1 has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v1.31 STN1 Sarah Leigh gene: STN1 was added
gene: STN1 was added to Cytopenia - NOT Fanconi anaemia. Sources: Literature
for-review tags were added to gene: STN1.
Mode of inheritance for gene: STN1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: STN1 were set to 27432940; 32627942
Phenotypes for gene: STN1 were set to Cerebroretinal microangiopathy with calcifications and cysts 2 OMIM:617341
Review for gene: STN1 was set to GREEN
Added comment: Comments from Zornitza Stark (Australian Genomics) Three individuals from unrelated families described with a multisystem disorder characterized by premature aging, pancytopaenia, hypocellular bone marrow, osteopenia, liver fibrosis, and vascular telangiectasia resulting in gastrointestinal bleeding, as well as intracranial calcifications and leukodystrophy, resulting in spasticity, ataxia, or dystonia. Gene belongs on multiple panels.
Sources: Literature
Cytopenia - NOT Fanconi anaemia v1.30 RPL9 Arina Puzriakova changed review comment from: Comment on list classification: Current Green rating is based on consensus from GLHs, so will remain Green. However, the 'for-review' tag has been added in view of the recent Red review by Zornitza Stark on this Green gene. ; to: Comment on list classification: Current Green rating is based on consensus from GLHs, so will remain Green. Excluding the VUS, only two unrelated cases published with the same variant, but including functional data. The 'for-review' tag has been added in view of this evidence and recent Red review by Zornitza Stark on a Green gene.
Cytopenia - NOT Fanconi anaemia v1.30 RPL9 Arina Puzriakova Tag for-review tag was added to gene: RPL9.
Cytopenia - NOT Fanconi anaemia v1.30 RPL9 Arina Puzriakova changed review comment from: Comment on list classification: Current Green rating is based on consensus from GLHs, so will remain Green.; to: Comment on list classification: Current Green rating is based on consensus from GLHs, so will remain Green. However, the 'for-review' tag has been added in view of the recent Red review by Zornitza Stark on this Green gene.
Cytopenia - NOT Fanconi anaemia v1.30 Catherine Snow List of related panels changed from R91; R258 to R91
Panel version has been signed off
Cytopenia - NOT Fanconi anaemia v1.29 EFL1 Catherine Snow Classified gene: EFL1 as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v1.29 EFL1 Catherine Snow Added comment: Comment on list classification: Changed rating to Amber to reflect NHS signed-off rating, will be reviewed at next major review.
Cytopenia - NOT Fanconi anaemia v1.29 EFL1 Catherine Snow Gene: efl1 has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v1.28 EFL1 Catherine Snow Tag for-review tag was added to gene: EFL1.
Cytopenia - NOT Fanconi anaemia v1.28 TINF2 Arina Puzriakova Phenotypes for gene: TINF2 were changed from Inherited Bone Marrow Failure Syndromes - Aplastic Anaemia; 268130 Revesz syndrome; Revesz Syndrome; Dyskeratosis Congenita, Autosomal Dominant, 3; DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 3; Dyskeratosis congenita; 613990 Dyskeratosis congenita, autosomal dominant 3; Dyskeratosis congenita, autosomal dominant 3, 613990; Revesz syndrome, 268130; Inherited Bone Marrow Failure Syndromes; Dyskeratosis Congenita, Dominant to Dyskeratosis congenita, autosomal dominant 3, 613990; Revesz syndrome, 268130; Inherited Bone Marrow Failure Syndromes - Aplastic Anaemia
Cytopenia - NOT Fanconi anaemia v1.27 RPS20 Arina Puzriakova Classified gene: RPS20 as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v1.27 RPS20 Arina Puzriakova Added comment: Comment on list classification: Rating Amber as currently only two unrelated cases reported with DBA in association with variants in the RPS20 gene (PMID:32790018).
Cytopenia - NOT Fanconi anaemia v1.27 RPS20 Arina Puzriakova Gene: rps20 has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v1.26 RPS20 Zornitza Stark gene: RPS20 was added
gene: RPS20 was added to Cytopenia - NOT Fanconi anaemia. Sources: Literature
Mode of inheritance for gene: RPS20 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: RPS20 were set to 32790018
Phenotypes for gene: RPS20 were set to Diamond Blackfan anaemia
Review for gene: RPS20 was set to AMBER
Added comment: Two unrelated cases where a de novo variant involving Ile84 (Ile84Ser and Ile84Asn), and reduce the RPS20 protein level in patient cells. Yeast models with mutation of the cognate residue resulted in defects in growth, ribosome biogenesis, and polysome formation. Loss of function may not be the mechanism of disease, because loss of function variants appear to be exclusively associated with familial colorectal cancer without the DBA phenotype.
Sources: Literature
Cytopenia - NOT Fanconi anaemia v1.26 RPL9 Arina Puzriakova Classified gene: RPL9 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v1.26 RPL9 Arina Puzriakova Added comment: Comment on list classification: Current Green rating is based on consensus from GLHs, so will remain Green.
Cytopenia - NOT Fanconi anaemia v1.26 RPL9 Arina Puzriakova Gene: rpl9 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v1.25 RPL9 Arina Puzriakova reviewed gene: RPL9: Rating: ; Mode of pathogenicity: None; Publications: 20116044, 29114930, 31799629; Phenotypes: Diamond Blackfan anaemia; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Cytopenia - NOT Fanconi anaemia v1.25 RPL26 Arina Puzriakova changed review comment from: To date, only a single individual has been reported with Diamond-Blackfan anemia due to a de novo 2-nucleotide deletion in RPL26. Includes some in vitro functional data indicating the variants impairs RPL26 function in ribosome biogenesis (PMID: 22431104); to: To date, only a single individual has been reported with Diamond-Blackfan anemia due to a de novo 2-nucleotide deletion in RPL26. Includes some in vitro functional data indicating the variant impairs RPL26 function in ribosome biogenesis (PMID: 22431104)
Cytopenia - NOT Fanconi anaemia v1.25 RPL26 Arina Puzriakova Tag for-review tag was added to gene: RPL26.
Cytopenia - NOT Fanconi anaemia v1.25 RPL26 Arina Puzriakova Classified gene: RPL26 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v1.25 RPL26 Arina Puzriakova Added comment: Comment on list classification: Current Green rating is based on consensus from GLHs, so will remain Green. However, this gene will be flagged for review at the date of next GMS panel update (added 'for-review' tag).
Cytopenia - NOT Fanconi anaemia v1.25 RPL26 Arina Puzriakova Gene: rpl26 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v1.24 RPL26 Arina Puzriakova reviewed gene: RPL26: Rating: ; Mode of pathogenicity: None; Publications: 22431104; Phenotypes: Diamond-Blackfan anemia 11, 614900; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Cytopenia - NOT Fanconi anaemia v1.24 NOP10 Arina Puzriakova Phenotypes for gene: NOP10 were changed from Dyskeratosis congenita, autosomal recessive 1, 224230; 224230 Dyskeratosis congenita, autosomal recessive 1 to Dyskeratosis congenita, autosomal recessive 1, 224230
Cytopenia - NOT Fanconi anaemia v1.23 NOP10 Arina Puzriakova reviewed gene: NOP10: Rating: ; Mode of pathogenicity: None; Publications: 17507419; Phenotypes: Dyskeratosis congenita, autosomal recessive 1, 224230; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v1.23 NHP2 Arina Puzriakova Phenotypes for gene: NHP2 were changed from 613987 Dyskeratosis congenita, autosomal recessive 2; Dyskeratosis congenita, autosomal recessive 2, 613987; Dyskeratosis congenita, autosomal recessive 2,613987 to Dyskeratosis congenita, autosomal recessive 2, 613987
Cytopenia - NOT Fanconi anaemia v1.22 NHP2 Arina Puzriakova Publications for gene: NHP2 were set to 18523010
Cytopenia - NOT Fanconi anaemia v1.21 NHP2 Arina Puzriakova Tag for-review tag was added to gene: NHP2.
Cytopenia - NOT Fanconi anaemia v1.21 NHP2 Arina Puzriakova Classified gene: NHP2 as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v1.21 NHP2 Arina Puzriakova Added comment: Comment on list classification: With addition of the recent paper flagged by Zornitza Stark (PMID:31985013), there is now a total of 3 unrelated cases with dyskeratosis congenita due to biallelic variants in NHP2, as well as supportive in vitro data.

Cases now reach threshold for inclusion and therefore, NHP2 should be promoted from Amber to Green at the next major review.
Cytopenia - NOT Fanconi anaemia v1.21 NHP2 Arina Puzriakova Gene: nhp2 has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v1.20 MYSM1 Arina Puzriakova Phenotypes for gene: MYSM1 were changed from 618116 Bone marrow failure syndrome 4 to Bone marrow failure syndrome 4, 618116
Cytopenia - NOT Fanconi anaemia v1.19 MYSM1 Arina Puzriakova Publications for gene: MYSM1 were set to
Cytopenia - NOT Fanconi anaemia v1.18 MYSM1 Arina Puzriakova Classified gene: MYSM1 as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v1.18 MYSM1 Arina Puzriakova Added comment: Comment on list classification: There are enough cases to support a gene-disease association, as well as several corroborative animal models. Therefore, there is sufficient evidence for MYSM1 to be upgraded from Amber to Green at the next major review.
Cytopenia - NOT Fanconi anaemia v1.18 MYSM1 Arina Puzriakova Gene: mysm1 has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v1.17 MYSM1 Arina Puzriakova Tag for-review tag was added to gene: MYSM1.
Cytopenia - NOT Fanconi anaemia v1.17 KIF23 Arina Puzriakova changed review comment from: Comment on list classification: Literature search showed KIF23 is a widely accepted cause of CDA type III, albeit only two families with the same variant have been published.

Furthermore, current Green rating based on consensus from GLHs, so will remain Green. However, this gene will be flagged for review at the date of next GMS panel update (added 'for-review' tag).; to: Comment on list classification: Literature search showed KIF23 is a widely accepted cause of CDA type III, albeit only two families with the same variant have been published.

Furthermore, current Green rating is based on consensus from GLHs, so will remain Green. However, this gene will be flagged for review at the date of next GMS panel update (added 'for-review' tag).
Cytopenia - NOT Fanconi anaemia v1.17 KIF23 Arina Puzriakova Tag for-review tag was added to gene: KIF23.
Cytopenia - NOT Fanconi anaemia v1.17 KIF23 Arina Puzriakova Classified gene: KIF23 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v1.17 KIF23 Arina Puzriakova Added comment: Comment on list classification: Literature search showed KIF23 is a widely accepted cause of CDA type III, albeit only two families with the same variant have been published.

Furthermore, current Green rating based on consensus from GLHs, so will remain Green. However, this gene will be flagged for review at the date of next GMS panel update (added 'for-review' tag).
Cytopenia - NOT Fanconi anaemia v1.17 KIF23 Arina Puzriakova Gene: kif23 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v1.16 KIF23 Arina Puzriakova reviewed gene: KIF23: Rating: ; Mode of pathogenicity: None; Publications: 23570799; Phenotypes: Congenital dyserythropoietic anemia type III; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Cytopenia - NOT Fanconi anaemia v1.16 DDX41 Arina Puzriakova Phenotypes for gene: DDX41 were changed from 616871 Susceptibility to myeloid neoplasms to Myeloproliferative/lymphoproliferative neoplasms, familial (multiple types), susceptibility to, 616871
Cytopenia - NOT Fanconi anaemia v1.15 DDX41 Arina Puzriakova Classified gene: DDX41 as Red List (low evidence)
Cytopenia - NOT Fanconi anaemia v1.15 DDX41 Arina Puzriakova Added comment: Comment on list classification: The rating of this gene should be re-evaluated by the GMS Haematology Specialist Test Group in context of the recent review by Zornitza Stark (added for-review tag)
Cytopenia - NOT Fanconi anaemia v1.15 DDX41 Arina Puzriakova Gene: ddx41 has been classified as Red List (Low Evidence).
Cytopenia - NOT Fanconi anaemia v1.14 DDX41 Arina Puzriakova Tag for-review tag was added to gene: DDX41.
Cytopenia - NOT Fanconi anaemia v1.14 SRP54 Arina Puzriakova Classified gene: SRP54 as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v1.14 SRP54 Arina Puzriakova Added comment: Comment on list classification: There is sufficient evidence to rate this gene GREEN at the next major review - at least 28 unrelated cases with congenital neutropenia due to variants in SRP54
Cytopenia - NOT Fanconi anaemia v1.14 SRP54 Arina Puzriakova Gene: srp54 has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v1.13 SRP54 Arina Puzriakova Added comment: Comment on publications: Added publications to support association with this phenotype.
Cytopenia - NOT Fanconi anaemia v1.13 SRP54 Arina Puzriakova Publications for gene: SRP54 were set to 28972538
Cytopenia - NOT Fanconi anaemia v1.12 SRP54 Arina Puzriakova Tag for-review tag was added to gene: SRP54.
Cytopenia - NOT Fanconi anaemia v1.12 SRP54 Arina Puzriakova Phenotypes for gene: SRP54 were changed from Syndromic neutropenia with Shwachman-Diamond-like features to Neutropenia, severe congenital, 8, autosomal dominant, 618752
Cytopenia - NOT Fanconi anaemia v1.11 NPM1 Arina Puzriakova Mode of inheritance for gene: NPM1 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to Unknown
Cytopenia - NOT Fanconi anaemia v1.10 NPM1 Arina Puzriakova Classified gene: NPM1 as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v1.10 NPM1 Arina Puzriakova Added comment: Comment on list classification: Rated Amber as additional cases required to corroborate causality and better define the phenotype. Both variants currently classified VUS - no information regarding segregation or zygosity.
Cytopenia - NOT Fanconi anaemia v1.10 NPM1 Arina Puzriakova Gene: npm1 has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v1.9 NPM1 Arina Puzriakova reviewed gene: NPM1: Rating: ; Mode of pathogenicity: None; Publications: 31570891; Phenotypes: Dyskeratosis congenita; Mode of inheritance: Unknown
Cytopenia - NOT Fanconi anaemia v1.9 AK2 Arina Puzriakova Phenotypes for gene: AK2 were changed from Reticular dysgenesis, MIM# 267500 to Reticular dysgenesis, 267500
Cytopenia - NOT Fanconi anaemia v1.8 AK2 Arina Puzriakova Added comment: Comment on publications: Added publications to support association with this phenotype.
Cytopenia - NOT Fanconi anaemia v1.8 AK2 Arina Puzriakova Publications for gene: AK2 were set to 19043416
Cytopenia - NOT Fanconi anaemia v1.7 AK2 Arina Puzriakova Classified gene: AK2 as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v1.7 AK2 Arina Puzriakova Added comment: Comment on list classification: There is sufficient evidence to rate this gene GREEN at the next major review - >3 unrelated cases with reticular dysgenesis (leukopenia is part of the phenotype) due to biallelic variants in AK2.
Cytopenia - NOT Fanconi anaemia v1.7 AK2 Arina Puzriakova Gene: ak2 has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v1.6 AK2 Arina Puzriakova Tag for-review tag was added to gene: AK2.
Cytopenia - NOT Fanconi anaemia v1.6 SRP54 Zornitza Stark gene: SRP54 was added
gene: SRP54 was added to Cytopenia - NOT Fanconi anaemia. Sources: Expert list
Mode of inheritance for gene: SRP54 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: SRP54 were set to 28972538
Phenotypes for gene: SRP54 were set to Syndromic neutropenia with Shwachman-Diamond-like features
Review for gene: SRP54 was set to GREEN
gene: SRP54 was marked as current diagnostic
Added comment: 3 unrelated families presented with neutropaenia associated with other symptoms, including exocrine pancreatic deficiency and/or autistic behavior, phenotypic overlap with Swachman-Diamond syndrome.
Sources: Expert list
Cytopenia - NOT Fanconi anaemia v1.6 RPL9 Zornitza Stark changed review comment from: PMID: 29114930, de novo splice site variant, c.-2+1G>C. Inherited missense variant reported in PMID 20116044, p.Arg125Ser is present in 31 hets in gnomad. PMID 23718193, cannot find RPL9 variant in main results table.; to: PMID: 29114930, de novo splice site variant, c.-2+1G>C, functional impact of this variant is likely deleterious but not proven. Inherited missense variant reported in PMID 20116044, p.Arg125Ser is present in 31 hets in gnomad. PMID 23718193, cannot find RPL9 variant in main results table.
Cytopenia - NOT Fanconi anaemia v1.6 RPL9 Zornitza Stark edited their review of gene: RPL9: Changed rating: RED
Cytopenia - NOT Fanconi anaemia v1.6 RPL9 Zornitza Stark changed review comment from: PMID: 29114930, de novo splice site variant, c.-2+1G>C. Inherited missense variant reported in PMID 20116044, p.Arg125Ser is present in 31 hets in gnomad. ; to: PMID: 29114930, de novo splice site variant, c.-2+1G>C. Inherited missense variant reported in PMID 20116044, p.Arg125Ser is present in 31 hets in gnomad. PMID 23718193, cannot find RPL9 variant in main results table.
Cytopenia - NOT Fanconi anaemia v1.6 RPL9 Zornitza Stark changed review comment from: PMID: 29114930, de novo splice site variant, c.-2+1G>C.; to: PMID: 29114930, de novo splice site variant, c.-2+1G>C. Inherited missense variant reported in PMID 20116044, p.Arg125Ser is present in 31 hets in gnomad.
Cytopenia - NOT Fanconi anaemia v1.6 RPL9 Zornitza Stark reviewed gene: RPL9: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Diamond Blackfan anaemia; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v1.6 RPL31 Zornitza Stark reviewed gene: RPL31: Rating: AMBER; Mode of pathogenicity: None; Publications: 25042156, 25424902; Phenotypes: Diamond Blackfan anaemia; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v1.6 RPL26 Zornitza Stark reviewed gene: RPL26: Rating: RED; Mode of pathogenicity: None; Publications: 22431104; Phenotypes: Diamond-Blackfan anemia 11, MIM# 614900; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v1.6 NPM1 Zornitza Stark gene: NPM1 was added
gene: NPM1 was added to Cytopenia - NOT Fanconi anaemia. Sources: Expert list
Mode of inheritance for gene: NPM1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: NPM1 were set to 31570891
Phenotypes for gene: NPM1 were set to radial ray defects; short stature; nail dsytrophy; bone marrow failure
Review for gene: NPM1 was set to GREEN
gene: NPM1 was marked as current diagnostic
Added comment: Two unrelated individuals with a dyskeratosis congenita phenotype and extensive functional data to support gene-disease relationship.
Sources: Expert list
Cytopenia - NOT Fanconi anaemia v1.6 NOP10 Zornitza Stark reviewed gene: NOP10: Rating: RED; Mode of pathogenicity: None; Publications: 17507419; Phenotypes: Dyskeratosis congenita, autosomal recessive 1, MIM#224230; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v1.6 NHP2 Zornitza Stark reviewed gene: NHP2: Rating: GREEN; Mode of pathogenicity: None; Publications: 18523010, 31985013; Phenotypes: Dyskeratosis congenita, autosomal recessive 2, MIM# 613987; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v1.6 MYSM1 Zornitza Stark reviewed gene: MYSM1: Rating: GREEN; Mode of pathogenicity: None; Publications: 24288411, 28115216, 26220525, 32640305; Phenotypes: Bone marrow failure syndrome 4, MIM#618116; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v1.6 KIF23 Zornitza Stark reviewed gene: KIF23: Rating: RED; Mode of pathogenicity: None; Publications: 23570799; Phenotypes: Congenital dyserythropoietic anemia type III; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v1.6 DDX41 Zornitza Stark reviewed gene: DDX41: Rating: GREEN; Mode of pathogenicity: None; Publications: 31698430, 31484648; Phenotypes: {Myeloproliferative/lymphoproliferative neoplasms, familial (multiple types), susceptibility to} MIM# 616871; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v1.6 AK2 Zornitza Stark gene: AK2 was added
gene: AK2 was added to Cytopenia - NOT Fanconi anaemia. Sources: Expert list
Mode of inheritance for gene: AK2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: AK2 were set to 19043416
Phenotypes for gene: AK2 were set to Reticular dysgenesis, MIM# 267500
Review for gene: AK2 was set to GREEN
gene: AK2 was marked as current diagnostic
Added comment: Well established gene-disease association.
Sources: Expert list
Cytopenia - NOT Fanconi anaemia v1.6 RPS29 Zornitza Stark reviewed gene: RPS29: Rating: AMBER; Mode of pathogenicity: None; Publications: 24829207; Phenotypes: Diamond-Blackfan anemia 13, MIM# 615909; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v1.6 EFL1 Catherine Snow Publications for gene: EFL1 were set to 29970384, 28331068
Cytopenia - NOT Fanconi anaemia v1.5 EFL1 Catherine Snow Classified gene: EFL1 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v1.5 EFL1 Catherine Snow Added comment: Comment on list classification: Upgrading to Green based on further individuals identified in publication PMID: 31151987
Cytopenia - NOT Fanconi anaemia v1.5 EFL1 Catherine Snow Gene: efl1 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v1.3 Catherine Snow Panel version has been signed off
Cytopenia - NOT Fanconi anaemia v1.2 Catherine Snow Panel types changed to GMS Rare Disease Virtual; GMS Rare Disease; GMS signed-off
Cytopenia - NOT Fanconi anaemia v1.0 Louise Daugherty promoted panel to version 1.0
Cytopenia - NOT Fanconi anaemia v0.137 Louise Daugherty Panel types changed to GMS Rare Disease; GMS signed-off
Cytopenia - NOT Fanconi anaemia v0.136 VWF Louise Daugherty Source Expert Review Red was added to VWF.
Cytopenia - NOT Fanconi anaemia v0.136 VPS13B Louise Daugherty Source Expert Review Red was added to VPS13B.
Cytopenia - NOT Fanconi anaemia v0.136 TUBB1 Louise Daugherty Source Expert Review Amber was added to TUBB1.
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.136 TCN2 Louise Daugherty Source Expert Review Amber was added to TCN2.
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.136 STK4 Louise Daugherty Source Expert Review Red was added to STK4.
Cytopenia - NOT Fanconi anaemia v0.136 STIM1 Louise Daugherty Source Expert Review Amber was added to STIM1.
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.136 SRC Louise Daugherty Source Expert Review Green was added to SRC.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.136 SLFN14 Louise Daugherty Source Expert Review Amber was added to SLFN14.
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.136 RUNX1 Louise Daugherty Source Expert Review Amber was added to RUNX1.
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.136 RNU4ATAC Louise Daugherty Source Expert Review Red was added to RNU4ATAC.
Cytopenia - NOT Fanconi anaemia v0.136 RBM8A Louise Daugherty Source Expert Review Red was added to RBM8A.
Rating Changed from Amber List (moderate evidence) to Red List (low evidence)
Cytopenia - NOT Fanconi anaemia v0.136 PTPN11 Louise Daugherty Source Expert Review Red was added to PTPN11.
Cytopenia - NOT Fanconi anaemia v0.136 PSMB8 Louise Daugherty Source Expert Review Red was added to PSMB8.
Cytopenia - NOT Fanconi anaemia v0.136 NBEAL2 Louise Daugherty Source Expert Review Amber was added to NBEAL2.
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.136 MYH9 Louise Daugherty Source Expert Review Amber was added to MYH9.
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.136 MTHFD1 Louise Daugherty Source Expert Review Red was added to MTHFD1.
Cytopenia - NOT Fanconi anaemia v0.136 MSN Louise Daugherty Source Expert Review Red was added to MSN.
Cytopenia - NOT Fanconi anaemia v0.136 MPIG6B Louise Daugherty Source Expert Review Red was added to MPIG6B.
Rating Changed from Amber List (moderate evidence) to Red List (low evidence)
Cytopenia - NOT Fanconi anaemia v0.136 LYST Louise Daugherty Source Expert Review Red was added to LYST.
Cytopenia - NOT Fanconi anaemia v0.136 LAMTOR2 Louise Daugherty Source Expert Review Red was added to LAMTOR2.
Cytopenia - NOT Fanconi anaemia v0.136 KDSR Louise Daugherty Source Expert Review Red was added to KDSR.
Cytopenia - NOT Fanconi anaemia v0.136 ITGB3 Louise Daugherty Source Expert Review Red was added to ITGB3.
Cytopenia - NOT Fanconi anaemia v0.136 ITGA2B Louise Daugherty Source Expert Review Red was added to ITGA2B.
Cytopenia - NOT Fanconi anaemia v0.136 HTRA2 Louise Daugherty Source Expert Review Red was added to HTRA2.
Cytopenia - NOT Fanconi anaemia v0.136 HOXA11 Louise Daugherty Source Expert Review Red was added to HOXA11.
Rating Changed from Amber List (moderate evidence) to Red List (low evidence)
Cytopenia - NOT Fanconi anaemia v0.136 GP9 Louise Daugherty Source Expert Review Amber was added to GP9.
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.136 GP1BB Louise Daugherty Source Expert Review Amber was added to GP1BB.
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.136 GP1BA Louise Daugherty Source Expert Review Amber was added to GP1BA.
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.136 GNE Louise Daugherty Source Expert Review Red was added to GNE.
Cytopenia - NOT Fanconi anaemia v0.136 GINS1 Louise Daugherty Source Expert Review Red was added to GINS1.
Cytopenia - NOT Fanconi anaemia v0.136 FLNA Louise Daugherty Source Expert Review Red was added to FLNA.
Cytopenia - NOT Fanconi anaemia v0.136 FLI1 Louise Daugherty Source Expert Review Amber was added to FLI1.
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.136 DIAPH1 Louise Daugherty Source Expert Review Red was added to DIAPH1.
Cytopenia - NOT Fanconi anaemia v0.136 CLPB Louise Daugherty Source Expert Review Red was added to CLPB.
Cytopenia - NOT Fanconi anaemia v0.136 CDC42 Louise Daugherty Source Expert Review Red was added to CDC42.
Cytopenia - NOT Fanconi anaemia v0.136 CD40LG Louise Daugherty Source Expert Review Red was added to CD40LG.
Cytopenia - NOT Fanconi anaemia v0.136 CD40 Louise Daugherty Source Expert Review Red was added to CD40.
Cytopenia - NOT Fanconi anaemia v0.136 ARPC1B Louise Daugherty Source Expert Review Red was added to ARPC1B.
Cytopenia - NOT Fanconi anaemia v0.136 AP3B1 Louise Daugherty Source Expert Review Amber was added to AP3B1.
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.136 ADAMTS13 Louise Daugherty Source Expert Review Amber was added to ADAMTS13.
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.136 ACTN1 Louise Daugherty Source Expert Review Amber was added to ACTN1.
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.136 ACTB Louise Daugherty Source Expert Review Red was added to ACTB.
Cytopenia - NOT Fanconi anaemia v0.136 ABCG8 Louise Daugherty Source Expert Review Amber was added to ABCG8.
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.136 ABCG5 Louise Daugherty Source Expert Review Amber was added to ABCG5.
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.135 WAS Louise Daugherty edited their review of gene: WAS: Added comment: Gene reviewed due to Haematology Specialist Test Group considering the inclusion of relevant neutropenia thrombocytopenia genes. The Specialist Test Group 21st October 2019 (consisting of 4 centres: WWMGLH, NWGLH, YNEGLH, LSGLH) all agreed that there is enough evidence to rate this gene Green. Additional comments from Haematology Specialist Test Group (Copy of Extra genes R91_consensus_v2.xlsx) 21st October 2019. Wessex and West Midlands GLH: Wiskott-Aldrich syndrome, can present as neonatal thrombocytopenia; North West GLH: no comment submitted; Yorkshire and North East GLH: no comment submitted; London South GLH: no comment submitted.; Changed rating: GREEN
Cytopenia - NOT Fanconi anaemia v0.135 VWF Louise Daugherty reviewed gene: VWF: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 VPS13B Louise Daugherty reviewed gene: VPS13B: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 TUBB1 Louise Daugherty commented on gene: TUBB1: Gene reviewed due to Haematology Specialist Test Group considering the inclusion of relevant neutropenia thrombocytopenia genes. The Specialist Test Group 21st October 2019 (consisting of 4 centres: WWMGLH, NWGLH, YNEGLH, LSGLH) all agreed that there was only enough evidence to rate this gene Amber. Additional comments from Haematology Specialist Test Group (Copy of Extra genes R91_consensus_v2.xlsx) 21st October 2019. Wessex and West Midlands GLH: Macrothrombocytopenia, beta-tubulin 1 related; North West GLH: Not isolated thrombocytopenia; Yorkshire and North East GLH: no comment submitted;London South GLH: no comment submitted.
Cytopenia - NOT Fanconi anaemia v0.135 THPO Louise Daugherty edited their review of gene: THPO: Added comment: Gene reviewed due to Haematology Specialist Test Group considering the inclusion of relevant neutropenia thrombocytopenia genes. The Specialist Test Group 21st October 2019 (consisting of 4 centres: WWMGLH, NWGLH, YNEGLH, LSGLH) all agreed that there is enough evidence to rate this gene Green. Additional comments from Haematology Specialist Test Group (Copy of Extra genes R91_consensus_v2.xlsx) 21st October 2019. Wessex and West Midlands GLH:Thrombocytopenia progressing to trilineage bone marrow failure; North West GLH: no comment submitted; Yorkshire and North East GLH: no comment submitted; London South GLH: no comment submitted.; Changed rating: GREEN
Cytopenia - NOT Fanconi anaemia v0.135 TCN2 Louise Daugherty reviewed gene: TCN2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 STK4 Louise Daugherty reviewed gene: STK4: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 STIM1 Louise Daugherty commented on gene: STIM1: Gene reviewed due to Haematology Specialist Test Group considering the inclusion of relevant neutropenia thrombocytopenia genes. The Specialist Test Group 21st October 2019 (consisting of 4 centres: WWMGLH, NWGLH, YNEGLH, LSGLH) all agreed that there was only enough evidence to rate this gene Amber. Additional comments from Haematology Specialist Test Group (Copy of Extra genes R91_consensus_v2.xlsx) 21st October 2019. Wessex and West Midlands GLH: Stormorken syndrome (York platelet syndrome); North West GLH: Syndromic, not isolated thrombocytopenia; Yorkshire and North East GLH: no commetn submitted; London South GLH: no comment submitted.
Cytopenia - NOT Fanconi anaemia v0.135 SRC Louise Daugherty reviewed gene: SRC: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 SMARCAL1 Louise Daugherty edited their review of gene: SMARCAL1: Added comment: Gene reviewed due to Haematology Specialist Test Group considering the inclusion of relevant neutropenia thrombocytopenia genes. The Specialist Test Group 21st October 2019 (consisting of 4 centres: WWMGLH, NWGLH, YNEGLH, LSGLH) all agree to rate this gene Red on this panel. Additional comments from Haematology Specialist Test Group (Copy of Extra genes R91_consensus_v2.xlsx) 21st October 2019. Wessex and West Midlands GLH: Multisystem disorder, skeletal defects seem to be consistently present, has not been associated with a cytopenia as presenting symptom; North West GLH:Syndromic, not isolated thrombocytopenia; Yorkshire and North East GLH:no comment submitted; London South GLH: no comment submitted; Changed rating: RED
Cytopenia - NOT Fanconi anaemia v0.135 SLFN14 Louise Daugherty reviewed gene: SLFN14: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 SLC37A4 Louise Daugherty edited their review of gene: SLC37A4: Added comment: Gene reviewed due to Haematology Specialist Test Group considering the inclusion of relevant neutropenia thrombocytopenia genes. The Specialist Test Group 21st October 2019 (consisting of 4 centres: WWMGLH, NWGLH, YNEGLH, LSGLH) all agree to rate this gene Red on this panel. Additional comments from Haematology Specialist Test Group (Copy of Extra genes R91_consensus_v2.xlsx) 21st October 2019. Wessex and West Midlands GLH: Glycogen storage disorders - other syndromic features (eg hypoglycaemia and splenomegaly) unlikely to present as neutropenia; North West GLH: Syndromic features, neutropenia, not isolated Thrombocytopenia; Yorkshire and North East GLH: no comment submitted; London South GLH: no comment submitted.; Changed rating: RED
Cytopenia - NOT Fanconi anaemia v0.135 RUNX1 Louise Daugherty commented on gene: RUNX1: Gene reviewed due to Haematology Specialist Test Group considering the inclusion of relevant neutropenia thrombocytopenia genes. The Specialist Test Group 21st October 2019 (consisting of 4 centres: WWMGLH, NWGLH, YNEGLH, LSGLH) all agreed that there was only enough evidence to rate this gene Amber. Additional comments from Haematology Specialist Test Group (Copy of Extra genes R91_consensus_v2.xlsx) 21st October 2019. Wessex and West Midlands GLH: Familial platelet disorder with predisposition to AML, typically presents with mild to moderate thrombocytopenia (normal sized platelets); North West GLH: Syndromic, not isolated thrombocytopenia; Yorkshire and North East GLH: no comment submitted; London South GLH: no comment submitted.
Cytopenia - NOT Fanconi anaemia v0.135 RNU4ATAC Louise Daugherty reviewed gene: RNU4ATAC: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 RBM8A Louise Daugherty edited their review of gene: RBM8A: Added comment: Gene reviewed due to Haematology Specialist Test Group considering the inclusion of relevant neutropenia thrombocytopenia genes. The Specialist Test Group 21st October 2019 (consisting of 4 centres: WWMGLH, NWGLH, YNEGLH, LSGLH) all agree to rate this gene Red on this panel. Additional comments from Haematology Specialist Test Group (Copy of Extra genes R91_consensus_v2.xlsx) 21st October 2019. Wessex and West Midlands GLH: Thrombocytopenia-absent radius syndrome (TAR); Thrombocytopenia is variable but skeletal abnormalities are always present so I would class red; however already agreed as Amber in July Update October: RBM8A is green on R90 (bleeding & platelet disorders panel), so its covered. Considering this, Id favour Red on R91 for consistency with other syndromic thrombocytopenia associated genes that weve considered for this panel; North West GLH: Syndromic, not isolated thrombocytopenia; Yorkshire and North East GLH: no comment submitted ;London South GLH: no comment submitted.; Changed rating: RED
Cytopenia - NOT Fanconi anaemia v0.135 PTPN11 Louise Daugherty reviewed gene: PTPN11: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 PSMB8 Louise Daugherty reviewed gene: PSMB8: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 NBEAL2 Louise Daugherty commented on gene: NBEAL2: Gene reviewed due to Haematology Specialist Test Group considering the inclusion of relevant neutropenia thrombocytopenia genes. The Specialist Test Group 21st October 2019 (consisting of 4 centres: WWMGLH, NWGLH, YNEGLH, LSGLH) all agreed that there was only enough evidence to rate this gene Amber. Additional comments from Haematology Specialist Test Group (Copy of Extra genes R91_consensus_v2.xlsx) 21st October 2019. Wessex and West Midlands GLH: Gray platelet syndrome; associated with low platelet count; North West GLH: Not isolated thrombocytopenia; Yorkshire and North East GLH:no comment submitted; London South GLH: no comment submitted.
Cytopenia - NOT Fanconi anaemia v0.135 MYH9 Louise Daugherty commented on gene: MYH9: Gene reviewed due to Haematology Specialist Test Group considering the inclusion of relevant neutropenia thrombocytopenia genes. The Specialist Test Group 21st October 2019 (consisting of 4 centres: WWMGLH, NWGLH, YNEGLH, LSGLH) all agreed that there was only enough evidence to rate this gene Amber. Additional comments from Haematology Specialist Test Group (Copy of Extra genes R91_consensus_v2.xlsx) 21st October 2019. Wessex and West Midlands GLH: May-Hegglin and other MYH9 disorders (macrothrombocytopenia plus other syndromic features); North West GLH: Syndromic, not isolated thrombocytopenia; Yorkshire and North East GLH: no comment submitted; London South GLH: no comment submitted.
Cytopenia - NOT Fanconi anaemia v0.135 MTHFD1 Louise Daugherty reviewed gene: MTHFD1: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 MSN Louise Daugherty reviewed gene: MSN: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 MPL Louise Daugherty edited their review of gene: MPL: Added comment: Gene reviewed due to Haematology Specialist Test Group considering the inclusion of relevant neutropenia thrombocytopenia genes. The Specialist Test Group 21st October 2019 (consisting of 4 centres: WWMGLH, NWGLH, YNEGLH, LSGLH) all agreed that there is enough evidence to rate this gene Green. Additional comments from Haematology Specialist Test Group (Copy of Extra genes R91_consensus_v2.xlsx) 21st October 2019. Wessex and West Midlands GLH: Congenital amegakaryocytic thrombocytopenia (CAMT) presents with isolated thrombocytopenia in infancy and developing into a pancytopenia in later childhood); North West GLH: no comment submitted; Yorkshire and North East GLH: no comment submitted; London South GLH: no comment submitted.; Changed rating: GREEN
Cytopenia - NOT Fanconi anaemia v0.135 MPIG6B Louise Daugherty edited their review of gene: MPIG6B: Added comment: Gene reviewed due to Haematology Specialist Test Group considering the inclusion of relevant neutropenia thrombocytopenia genes. The Specialist Test Group 21st October 2019 (consisting of 4 centres: WWMGLH, NWGLH, YNEGLH, LSGLH) all agree to rate this gene Red on this panel. Additional comments from Haematology Specialist Test Group (Copy of Extra genes R91_consensus_v2.xlsx) 21st October 2019. Wessex and West Midlands GLH: Typically Thrombocytopenia, anemia and myelofibrosis (myelofibrosis is a distinct phenotype that is not targeted by this panel) - but one case of child presenting with pancytopenia; North West GLH: Syndromic, not isolated thrombocytopenia; Yorkshire and North East GLH: no comment submitted; London South GLH: no comment submitted.; Changed rating: RED
Cytopenia - NOT Fanconi anaemia v0.135 MECOM Louise Daugherty edited their review of gene: MECOM: Added comment: Gene reviewed due to Haematology Specialist Test Group considering the inclusion of relevant neutropenia thrombocytopenia genes. The Specialist Test Group 21st October 2019 (consisting of 4 centres: WWMGLH, NWGLH, YNEGLH, LSGLH) all agreed that there is enough evidence to rate this gene Green. Additional comments from Haematology Specialist Test Group (Copy of Extra genes R91_consensus_v2.xlsx) 21st October 2019. Wessex and West Midlands GLH: Clinical spectrum ranged from isolated radioulnar synostosis with no or mild hematological involvement to severe bone marrow failure without obvious skeletal abnormality. Germeshausen 2018;North West GLH: no comment submitted; Yorkshire and North East GLH: no comment submitted; London South GLH: no comment submitted.; Changed rating: GREEN
Cytopenia - NOT Fanconi anaemia v0.135 LYST Louise Daugherty reviewed gene: LYST: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 LAMTOR2 Louise Daugherty reviewed gene: LAMTOR2: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 KDSR Louise Daugherty reviewed gene: KDSR: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 ITGB3 Louise Daugherty reviewed gene: ITGB3: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 ITGA2B Louise Daugherty reviewed gene: ITGA2B: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 HTRA2 Louise Daugherty reviewed gene: HTRA2: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 HOXA11 Louise Daugherty edited their review of gene: HOXA11: Added comment: Gene reviewed due to Haematology Specialist Test Group considering the inclusion of relevant neutropenia thrombocytopenia genes. The Specialist Test Group 21st October 2019 (consisting of 4 centres: WWMGLH, NWGLH, YNEGLH, LSGLH) all agree to rate this gene Red on this panel. Additional comments from Haematology Specialist Test Group (Copy of Extra genes R91_consensus_v2.xlsx) 21st October 2019. Wessex and West Midlands GLH: Amegakaryocytic thrombocytopenia with radioulnar synostosis; so far has always been described in combination with obvious skeletal defect; North West GLH: Syndromic, not isolated thrombocytopenia; Yorkshire and North East GLH: no comment submitted; London South GLH: no comment submitted.; Changed rating: RED
Cytopenia - NOT Fanconi anaemia v0.135 GP9 Louise Daugherty reviewed gene: GP9: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 GP1BB Louise Daugherty reviewed gene: GP1BB: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 GP1BA Louise Daugherty commented on gene: GP1BA: Gene reviewed due to Haematology Specialist Test Group considering the inclusion of relevant neutropenia thrombocytopenia genes. The Specialist Test Group 21st October 2019 (consisting of 4 centres: WWMGLH, NWGLH, YNEGLH, LSGLH) all agreed that there was only enough evidence to rate this gene Amber. Additional comments from Haematology Specialist Test Group (Copy of Extra genes R91_consensus_v2.xlsx) 21st October 2019. Wessex and West Midlands GLH: Mild macrothrombocytopenia; North West GLH: Platelet type VWD, mild thrombocytopenia; Yorkshire and North East GLH: no comment submitted; London South GLH: no comment submitted.
Cytopenia - NOT Fanconi anaemia v0.135 GNE Louise Daugherty reviewed gene: GNE: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 GINS1 Louise Daugherty reviewed gene: GINS1: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 GFI1 Louise Daugherty edited their review of gene: GFI1: Added comment: Gene reviewed due to Haematology Specialist Test Group considering the inclusion of relevant neutropenia thrombocytopenia genes. The Specialist Test Group 21st October 2019 (consisting of 4 centres: WWMGLH, NWGLH, YNEGLH, LSGLH) all agreed that there is enough evidence to rate this gene Green. Additional comments from Haematology Specialist Test Group (Copy of Extra genes R91_consensus_v2.xlsx) 21st October 2019. Wessex and West Midlands GLH: Platelet type bleeding disorder 17; Severe congenital neutropenia 2; North West GLH: no comment submitted; Yorkshire and North East GLH: only 2 changes on HGMD neutropenia; London South GLH: no comment submitted. ; Changed rating: GREEN
Cytopenia - NOT Fanconi anaemia v0.135 GATA1 Louise Daugherty edited their review of gene: GATA1: Added comment: Gene reviewed due to Haematology Specialist Test Group considering the inclusion of relevant neutropenia thrombocytopenia genes. The Specialist Test Group 21st October 2019 (consisting of 4 centres: WWMGLH, NWGLH, YNEGLH, LSGLH) all agreed that there is enough evidence to rate this gene Green. Additional comments from Haematology Specialist Test Group (Copy of Extra genes R91_consensus_v2.xlsx) 21st October 2019. Wessex and West Midlands GLH: X-linked thrombocytopenia with dyserythropoiesis; North West GLH: no comment submitted; Yorkshire and North East GLH: no comment submitted; London South GLH: no comment submitted. ; Changed rating: GREEN
Cytopenia - NOT Fanconi anaemia v0.135 FYB1 Louise Daugherty edited their review of gene: FYB1: Added comment: Gene reviewed due to Haematology Specialist Test Group considering the inclusion of relevant neutropenia thrombocytopenia genes. The Specialist Test Group 21st October 2019 (consisting of 4 centres: WWMGLH, NWGLH, YNEGLH, LSGLH) all agreed that there is enough evidence to rate this gene Green. Additional comments from Haematology Specialist Test Group (Copy of Extra genes R91_consensus_v2.xlsx) 21st October 2019. Wessex and West Midlands GLH: Thrombocytopenia 3; North West GLH: no comment submitted; Yorkshire and North East GLH: Rare (2cases); London South GLH: no comment submitted.; Changed rating: GREEN
Cytopenia - NOT Fanconi anaemia v0.135 FLNA Louise Daugherty reviewed gene: FLNA: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 FLI1 Louise Daugherty reviewed gene: FLI1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 ETV6 Louise Daugherty edited their review of gene: ETV6: Added comment: Gene reviewed due to Haematology Specialist Test Group considering the inclusion of relevant neutropenia thrombocytopenia genes. The Specialist Test Group 21st October 2019 (consisting of 4 centres: WWMGLH, NWGLH, YNEGLH, LSGLH) all agreed that there is enough evidence to rate this gene Green. Additional comments from Haematology Specialist Test Group (Copy of Extra genes R91_consensus_v2.xlsx) 21st October 2019. Wessex and West Midlands GLH: Thrombocytopenia and susceptibility to cancer; North West GLH: no comment submitted; Yorkshire and North East GLH:mainly somatic AML and some thrombocytopenia; London South GLH: no comment submitted.; Changed rating: GREEN
Cytopenia - NOT Fanconi anaemia v0.135 DIAPH1 Louise Daugherty reviewed gene: DIAPH1: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 CYCS Louise Daugherty edited their review of gene: CYCS: Added comment: Gene reviewed due to Haematology Specialist Test Group considering the inclusion of relevant neutropenia thrombocytopenia genes. The Specialist Test Group 21st October 2019 (consisting of 4 centres: WWMGLH, NWGLH, YNEGLH, LSGLH) all agreed that there is enough evidence to rate this gene Green. Additional comments from Haematology Specialist Test Group (Copy of Extra genes R91_consensus_v2.xlsx) 21st October 2019. Wessex and West Midlands GLH: Autosomal dominant thrombocytopenia 4; North West GLH: no comment submitted; Yorkshire and North East GLH: rare (4 cases); London South GLH: no comment submitted.; Changed rating: GREEN
Cytopenia - NOT Fanconi anaemia v0.135 CLPB Louise Daugherty reviewed gene: CLPB: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 CDC42 Louise Daugherty reviewed gene: CDC42: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 CD40LG Louise Daugherty reviewed gene: CD40LG: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 CD40 Louise Daugherty reviewed gene: CD40: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 ARPC1B Louise Daugherty reviewed gene: ARPC1B: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 AP3B1 Louise Daugherty reviewed gene: AP3B1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 ANKRD26 Louise Daugherty edited their review of gene: ANKRD26: Added comment: Gene reviewed due to Haematology Specialist Test Group considering the inclusion of relevant neutropenia thrombocytopenia genes. The Specialist Test Group 21st October 2019 (consisting of 4 centres: WWMGLH, NWGLH, YNEGLH, LSGLH) all agreed that there is enough evidence to rate this gene Green. Additional comments from Haematology Specialist Test Group (Copy of Extra genes R91_consensus_v2.xlsx) 21st October 2019. Wessex and West Midlands GLH: Autosomal dominant thrombocytopenia 2; North West GLH: TTP and Upshaw-Schulman syndrome (recessive TTP); Yorkshire and North East GLH: no comment submitted; London South GLH: no comment submitted. ; Changed rating: GREEN
Cytopenia - NOT Fanconi anaemia v0.135 ADAMTS13 Louise Daugherty reviewed gene: ADAMTS13: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 ACTN1 Louise Daugherty reviewed gene: ACTN1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 ACTB Louise Daugherty reviewed gene: ACTB: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 ABCG8 Louise Daugherty reviewed gene: ABCG8: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.135 ABCG5 Louise Daugherty reviewed gene: ABCG5: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.134 WAS Louise Daugherty Source Expert review Green was added to WAS.
Cytopenia - NOT Fanconi anaemia v0.134 VWF Louise Daugherty Source Expert review Red was added to VWF.
Cytopenia - NOT Fanconi anaemia v0.134 VPS13B Louise Daugherty Source Expert review Red was added to VPS13B.
Cytopenia - NOT Fanconi anaemia v0.134 TUBB1 Louise Daugherty Source Expert review Amber was added to TUBB1.
Cytopenia - NOT Fanconi anaemia v0.134 THPO Louise Daugherty Source Expert review Green was added to THPO.
Cytopenia - NOT Fanconi anaemia v0.134 TCN2 Louise Daugherty Source Expert review Amber was added to TCN2.
Cytopenia - NOT Fanconi anaemia v0.134 STK4 Louise Daugherty Source Expert review Red was added to STK4.
Cytopenia - NOT Fanconi anaemia v0.134 STIM1 Louise Daugherty Source Expert review Amber was added to STIM1.
Cytopenia - NOT Fanconi anaemia v0.134 SRC Louise Daugherty Source Expert review Green was added to SRC.
Cytopenia - NOT Fanconi anaemia v0.134 SMARCAL1 Louise Daugherty Source Expert review Red was added to SMARCAL1.
Cytopenia - NOT Fanconi anaemia v0.134 SLFN14 Louise Daugherty Source Expert review Amber was added to SLFN14.
Cytopenia - NOT Fanconi anaemia v0.134 SLC37A4 Louise Daugherty Source Expert review Red was added to SLC37A4.
Cytopenia - NOT Fanconi anaemia v0.134 RUNX1 Louise Daugherty Source Expert review Amber was added to RUNX1.
Cytopenia - NOT Fanconi anaemia v0.134 RNU4ATAC Louise Daugherty Source Expert review Red was added to RNU4ATAC.
Cytopenia - NOT Fanconi anaemia v0.134 RBM8A Louise Daugherty Source Expert review Red was added to RBM8A.
Cytopenia - NOT Fanconi anaemia v0.134 PTPN11 Louise Daugherty Source Expert review Red was added to PTPN11.
Cytopenia - NOT Fanconi anaemia v0.134 PSMB8 Louise Daugherty Source Expert review Red was added to PSMB8.
Cytopenia - NOT Fanconi anaemia v0.134 NBEAL2 Louise Daugherty Source Expert review Amber was added to NBEAL2.
Cytopenia - NOT Fanconi anaemia v0.134 MYH9 Louise Daugherty Source Expert review Amber was added to MYH9.
Cytopenia - NOT Fanconi anaemia v0.134 MTHFD1 Louise Daugherty Source Expert review Red was added to MTHFD1.
Cytopenia - NOT Fanconi anaemia v0.134 MSN Louise Daugherty Source Expert review Red was added to MSN.
Cytopenia - NOT Fanconi anaemia v0.134 MPL Louise Daugherty Source Expert review Green was added to MPL.
Cytopenia - NOT Fanconi anaemia v0.134 MPIG6B Louise Daugherty Source Expert review Red was added to MPIG6B.
Cytopenia - NOT Fanconi anaemia v0.134 MECOM Louise Daugherty Source Expert review Green was added to MECOM.
Cytopenia - NOT Fanconi anaemia v0.134 LYST Louise Daugherty Source Expert review Red was added to LYST.
Cytopenia - NOT Fanconi anaemia v0.134 LAMTOR2 Louise Daugherty Source Expert review Red was added to LAMTOR2.
Cytopenia - NOT Fanconi anaemia v0.134 KDSR Louise Daugherty Source Expert review Red was added to KDSR.
Cytopenia - NOT Fanconi anaemia v0.134 ITGB3 Louise Daugherty Source Expert review Red was added to ITGB3.
Cytopenia - NOT Fanconi anaemia v0.134 ITGA2B Louise Daugherty Source Expert review Red was added to ITGA2B.
Cytopenia - NOT Fanconi anaemia v0.134 HTRA2 Louise Daugherty Source Expert review Red was added to HTRA2.
Cytopenia - NOT Fanconi anaemia v0.134 HOXA11 Louise Daugherty Source Expert review Red was added to HOXA11.
Cytopenia - NOT Fanconi anaemia v0.134 GP9 Louise Daugherty Source Expert review Amber was added to GP9.
Cytopenia - NOT Fanconi anaemia v0.134 GP1BB Louise Daugherty Source Expert review Amber was added to GP1BB.
Cytopenia - NOT Fanconi anaemia v0.134 GP1BA Louise Daugherty Source Expert review Amber was added to GP1BA.
Cytopenia - NOT Fanconi anaemia v0.134 GNE Louise Daugherty Source Expert review Red was added to GNE.
Cytopenia - NOT Fanconi anaemia v0.134 GINS1 Louise Daugherty Source Expert review Red was added to GINS1.
Cytopenia - NOT Fanconi anaemia v0.134 GFI1 Louise Daugherty Source Expert review Green was added to GFI1.
Cytopenia - NOT Fanconi anaemia v0.134 GATA1 Louise Daugherty Source Expert review Green was added to GATA1.
Cytopenia - NOT Fanconi anaemia v0.134 FYB1 Louise Daugherty Source Expert review Green was added to FYB1.
Cytopenia - NOT Fanconi anaemia v0.134 FLNA Louise Daugherty Source Expert review Red was added to FLNA.
Cytopenia - NOT Fanconi anaemia v0.134 FLI1 Louise Daugherty Source Expert review Amber was added to FLI1.
Cytopenia - NOT Fanconi anaemia v0.134 ETV6 Louise Daugherty Source Expert review Green was added to ETV6.
Cytopenia - NOT Fanconi anaemia v0.134 DIAPH1 Louise Daugherty Source Expert review Red was added to DIAPH1.
Cytopenia - NOT Fanconi anaemia v0.134 CYCS Louise Daugherty Source Expert review Green was added to CYCS.
Cytopenia - NOT Fanconi anaemia v0.134 CLPB Louise Daugherty Source Expert review Red was added to CLPB.
Cytopenia - NOT Fanconi anaemia v0.134 CDC42 Louise Daugherty Source Expert review Red was added to CDC42.
Cytopenia - NOT Fanconi anaemia v0.134 CD40LG Louise Daugherty Source Expert review Red was added to CD40LG.
Cytopenia - NOT Fanconi anaemia v0.134 CD40 Louise Daugherty Source Expert review Red was added to CD40.
Cytopenia - NOT Fanconi anaemia v0.134 ARPC1B Louise Daugherty Source Expert review Red was added to ARPC1B.
Cytopenia - NOT Fanconi anaemia v0.134 AP3B1 Louise Daugherty Source Expert review Amber was added to AP3B1.
Cytopenia - NOT Fanconi anaemia v0.134 ANKRD26 Louise Daugherty Source Expert review Green was added to ANKRD26.
Cytopenia - NOT Fanconi anaemia v0.134 ADAMTS13 Louise Daugherty Source Expert review Amber was added to ADAMTS13.
Cytopenia - NOT Fanconi anaemia v0.134 ACTN1 Louise Daugherty Source Expert review Amber was added to ACTN1.
Cytopenia - NOT Fanconi anaemia v0.134 ACTB Louise Daugherty Source Expert review Red was added to ACTB.
Cytopenia - NOT Fanconi anaemia v0.134 ABCG8 Louise Daugherty Source Expert review Amber was added to ABCG8.
Cytopenia - NOT Fanconi anaemia v0.134 ABCG5 Louise Daugherty Source Expert review Amber was added to ABCG5.
Cytopenia - NOT Fanconi anaemia v0.133 VWF Louise Daugherty Mode of inheritance for gene VWF was changed from to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Added phenotypes von Willebrand disease, types 2A, 2B, 2M, and 2N, 613554; von Willibrand disease, type 3, 277480; von Willebrand disease, type 1, 193400 for gene: VWF
Cytopenia - NOT Fanconi anaemia v0.133 VPS13B Louise Daugherty Mode of inheritance for gene VPS13B was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Cohen syndrome, 216550 for gene: VPS13B
Cytopenia - NOT Fanconi anaemia v0.133 TCN2 Louise Daugherty Mode of inheritance for gene TCN2 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Transcobalamin II deficiency, 275350 for gene: TCN2
Cytopenia - NOT Fanconi anaemia v0.133 STK4 Louise Daugherty Mode of inheritance for gene STK4 was changed from to Unknown
Added phenotypes T-cell immunodeficiency, recurrent infections, autoimmunity, and cardiac malformations, 614868 for gene: STK4
Cytopenia - NOT Fanconi anaemia v0.133 SRC Louise Daugherty Mode of inheritance for gene SRC was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Added phenotypes ?Thrombocytopenia 6, 616937 for gene: SRC
Cytopenia - NOT Fanconi anaemia v0.133 SLFN14 Louise Daugherty Mode of inheritance for gene SLFN14 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Added phenotypes Bleeding disorder, platelet-type, 20, 616913 for gene: SLFN14
Cytopenia - NOT Fanconi anaemia v0.133 RNU4ATAC Louise Daugherty Mode of inheritance for gene RNU4ATAC was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Roifman syndrome, 616651; Microcephalic osteodysplastic primordial dwarfism, type I, 210710 for gene: RNU4ATAC
Cytopenia - NOT Fanconi anaemia v0.133 PTPN11 Louise Daugherty Mode of inheritance for gene PTPN11 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Added phenotypes Noonan syndrome 1, 163950 for gene: PTPN11
Cytopenia - NOT Fanconi anaemia v0.133 PSMB8 Louise Daugherty Mode of inheritance for gene PSMB8 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Proteasome-associated autoinflammatory syndrome 1 and digenic forms, 256040 for gene: PSMB8
Cytopenia - NOT Fanconi anaemia v0.133 MTHFD1 Louise Daugherty Mode of inheritance for gene MTHFD1 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia, 617780 for gene: MTHFD1
Cytopenia - NOT Fanconi anaemia v0.133 MSN Louise Daugherty Mode of inheritance for gene MSN was changed from to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Added phenotypes Immunodeficiency 50, 300988 for gene: MSN
Cytopenia - NOT Fanconi anaemia v0.133 LYST Louise Daugherty Mode of inheritance for gene LYST was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Chediak-Higashi syndrome, 214500 for gene: LYST
Cytopenia - NOT Fanconi anaemia v0.133 LAMTOR2 Louise Daugherty Mode of inheritance for gene LAMTOR2 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Immunodeficiency due to defect in MAPBP-interacting protein, 610798 for gene: LAMTOR2
Cytopenia - NOT Fanconi anaemia v0.133 KDSR Louise Daugherty Mode of inheritance for gene KDSR was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Erythrokeratodermia variabilis et progressiva 4, 617526 for gene: KDSR
Cytopenia - NOT Fanconi anaemia v0.133 ITGB3 Louise Daugherty Mode of inheritance for gene ITGB3 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Glanzmann thrombasthenia, 273800 for gene: ITGB3
Cytopenia - NOT Fanconi anaemia v0.133 ITGA2B Louise Daugherty Mode of inheritance for gene ITGA2B was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Glanzmann thrombasthenia, 273800 for gene: ITGA2B
Cytopenia - NOT Fanconi anaemia v0.133 HTRA2 Louise Daugherty Mode of inheritance for gene HTRA2 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes 3-methylglutaconic aciduria, type VIII, 617248 for gene: HTRA2
Cytopenia - NOT Fanconi anaemia v0.133 GP9 Louise Daugherty Mode of inheritance for gene GP9 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Bernard-Soulier syndrome (includes macrothrombocytopenia); Bernard-Soulier syndrome, type C, 231200 for gene: GP9
Cytopenia - NOT Fanconi anaemia v0.133 GP1BB Louise Daugherty Mode of inheritance for gene GP1BB was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Bernard-Soulier syndrome, type B, 231200; Mild macrothrombocytopenia for gene: GP1BB
Cytopenia - NOT Fanconi anaemia v0.133 GNE Louise Daugherty Mode of inheritance for gene GNE was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Nonaka myopathy, 605820 for gene: GNE
Cytopenia - NOT Fanconi anaemia v0.133 GINS1 Louise Daugherty Mode of inheritance for gene GINS1 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Immunodeficiency 55, 617827 for gene: GINS1
Cytopenia - NOT Fanconi anaemia v0.133 FLNA Louise Daugherty Mode of inheritance for gene FLNA was changed from to Unknown
Cytopenia - NOT Fanconi anaemia v0.133 FLI1 Louise Daugherty Mode of inheritance for gene FLI1 was changed from to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Added phenotypes Bleeding disorder, platelet-type, 21, 617443 for gene: FLI1
Cytopenia - NOT Fanconi anaemia v0.133 DIAPH1 Louise Daugherty Mode of inheritance for gene DIAPH1 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Added phenotypes Macrothrombocytopenia and hearing loss; Deafness, autosomal dominant 1, 124900 for gene: DIAPH1
Cytopenia - NOT Fanconi anaemia v0.133 CLPB Louise Daugherty Mode of inheritance for gene CLPB was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes 3-methylglutaconic aciduria, type VII, with cataracts, neurologic involvement and neutropenia, 616271 for gene: CLPB
Cytopenia - NOT Fanconi anaemia v0.133 CDC42 Louise Daugherty Mode of inheritance for gene CDC42 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Added phenotypes Takenouchi-Kosaki syndrome, 616737 for gene: CDC42
Cytopenia - NOT Fanconi anaemia v0.133 CD40LG Louise Daugherty Mode of inheritance for gene CD40LG was changed from to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Added phenotypes Immunodeficiency, X-linked, with hyper-IgM, 308230 for gene: CD40LG
Cytopenia - NOT Fanconi anaemia v0.133 CD40 Louise Daugherty Mode of inheritance for gene CD40 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Immunodeficiency with hyper-IgM, type 3, 606843 for gene: CD40
Cytopenia - NOT Fanconi anaemia v0.133 ARPC1B Louise Daugherty Mode of inheritance for gene ARPC1B was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Platelet abnormalities with eosinophilia and immune-mediated inflammatory disease, 617718 for gene: ARPC1B
Cytopenia - NOT Fanconi anaemia v0.133 AP3B1 Louise Daugherty Mode of inheritance for gene AP3B1 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Hermansky-Pudlak syndrome 2, 608233 for gene: AP3B1
Cytopenia - NOT Fanconi anaemia v0.133 ADAMTS13 Louise Daugherty Mode of inheritance for gene ADAMTS13 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Thrombotic thrombocytopenic purpura, familial, 274150 for gene: ADAMTS13
Cytopenia - NOT Fanconi anaemia v0.133 ACTN1 Louise Daugherty Mode of inheritance for gene ACTN1 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Added phenotypes Bleeding disorder, platelet-type, 15, 615193; Macrothrombocytopenia for gene: ACTN1
Cytopenia - NOT Fanconi anaemia v0.133 ACTB Louise Daugherty Mode of inheritance for gene ACTB was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Added phenotypes Baraitser-Winter syndrome 1 with macrothrombocytopenia; Baraitser-Winter syndrome 1, 243310 for gene: ACTB
Cytopenia - NOT Fanconi anaemia v0.133 ABCG8 Louise Daugherty Mode of inheritance for gene ABCG8 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Sitosterolemia with macrothrombocytopenia; Sitosterolemia, 210250 for gene: ABCG8
Cytopenia - NOT Fanconi anaemia v0.133 ABCG5 Louise Daugherty Mode of inheritance for gene ABCG5 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Sitosterolemia with macrothrombocytopenia; Sitosterolemia, 210250 for gene: ABCG5
Cytopenia - NOT Fanconi anaemia v0.132 VWF Louise Daugherty gene: VWF was added
gene: VWF was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: VWF was set to
Cytopenia - NOT Fanconi anaemia v0.132 VPS13B Louise Daugherty gene: VPS13B was added
gene: VPS13B was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: VPS13B was set to
Cytopenia - NOT Fanconi anaemia v0.132 TUBB1 Louise Daugherty Source Wessex and West Midlands GLH was added to TUBB1.
Source Yorkshire and North East GLH was added to TUBB1.
Source North West GLH was added to TUBB1.
Cytopenia - NOT Fanconi anaemia v0.132 THPO Louise Daugherty Source Wessex and West Midlands GLH was added to THPO.
Cytopenia - NOT Fanconi anaemia v0.132 TCN2 Louise Daugherty gene: TCN2 was added
gene: TCN2 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: TCN2 was set to
Cytopenia - NOT Fanconi anaemia v0.132 STK4 Louise Daugherty gene: STK4 was added
gene: STK4 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: STK4 was set to
Cytopenia - NOT Fanconi anaemia v0.132 STIM1 Louise Daugherty Source Wessex and West Midlands GLH was added to STIM1.
Source Yorkshire and North East GLH was added to STIM1.
Source North West GLH was added to STIM1.
Cytopenia - NOT Fanconi anaemia v0.132 SRC Louise Daugherty gene: SRC was added
gene: SRC was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: SRC was set to
Cytopenia - NOT Fanconi anaemia v0.132 SMARCAL1 Louise Daugherty Source Wessex and West Midlands GLH was added to SMARCAL1.
Source Yorkshire and North East GLH was added to SMARCAL1.
Source North West GLH was added to SMARCAL1.
Cytopenia - NOT Fanconi anaemia v0.132 SLFN14 Louise Daugherty gene: SLFN14 was added
gene: SLFN14 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: SLFN14 was set to
Cytopenia - NOT Fanconi anaemia v0.132 SLC37A4 Louise Daugherty Source Wessex and West Midlands GLH was added to SLC37A4.
Source Yorkshire and North East GLH was added to SLC37A4.
Source North West GLH was added to SLC37A4.
Cytopenia - NOT Fanconi anaemia v0.132 RUNX1 Louise Daugherty Source Wessex and West Midlands GLH was added to RUNX1.
Source Yorkshire and North East GLH was added to RUNX1.
Source North West GLH was added to RUNX1.
Cytopenia - NOT Fanconi anaemia v0.132 RNU4ATAC Louise Daugherty gene: RNU4ATAC was added
gene: RNU4ATAC was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: RNU4ATAC was set to
Cytopenia - NOT Fanconi anaemia v0.132 RBM8A Louise Daugherty Source Wessex and West Midlands GLH was added to RBM8A.
Cytopenia - NOT Fanconi anaemia v0.132 PTPN11 Louise Daugherty gene: PTPN11 was added
gene: PTPN11 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: PTPN11 was set to
Cytopenia - NOT Fanconi anaemia v0.132 PSMB8 Louise Daugherty gene: PSMB8 was added
gene: PSMB8 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: PSMB8 was set to
Cytopenia - NOT Fanconi anaemia v0.132 NBEAL2 Louise Daugherty Source Wessex and West Midlands GLH was added to NBEAL2.
Source Yorkshire and North East GLH was added to NBEAL2.
Source North West GLH was added to NBEAL2.
Cytopenia - NOT Fanconi anaemia v0.132 MYH9 Louise Daugherty Source Wessex and West Midlands GLH was added to MYH9.
Source Yorkshire and North East GLH was added to MYH9.
Source North West GLH was added to MYH9.
Cytopenia - NOT Fanconi anaemia v0.132 MTHFD1 Louise Daugherty gene: MTHFD1 was added
gene: MTHFD1 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: MTHFD1 was set to
Cytopenia - NOT Fanconi anaemia v0.132 MSN Louise Daugherty gene: MSN was added
gene: MSN was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: MSN was set to
Cytopenia - NOT Fanconi anaemia v0.132 MPL Louise Daugherty Source Wessex and West Midlands GLH was added to MPL.
Cytopenia - NOT Fanconi anaemia v0.132 MPIG6B Louise Daugherty Source Yorkshire and North East GLH was added to MPIG6B.
Cytopenia - NOT Fanconi anaemia v0.132 MECOM Louise Daugherty Source Wessex and West Midlands GLH was added to MECOM.
Cytopenia - NOT Fanconi anaemia v0.132 LYST Louise Daugherty gene: LYST was added
gene: LYST was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: LYST was set to
Cytopenia - NOT Fanconi anaemia v0.132 LAMTOR2 Louise Daugherty gene: LAMTOR2 was added
gene: LAMTOR2 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: LAMTOR2 was set to
Cytopenia - NOT Fanconi anaemia v0.132 KDSR Louise Daugherty gene: KDSR was added
gene: KDSR was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: KDSR was set to
Cytopenia - NOT Fanconi anaemia v0.132 ITGB3 Louise Daugherty gene: ITGB3 was added
gene: ITGB3 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: ITGB3 was set to
Cytopenia - NOT Fanconi anaemia v0.132 ITGA2B Louise Daugherty gene: ITGA2B was added
gene: ITGA2B was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: ITGA2B was set to
Cytopenia - NOT Fanconi anaemia v0.132 HTRA2 Louise Daugherty gene: HTRA2 was added
gene: HTRA2 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: HTRA2 was set to
Cytopenia - NOT Fanconi anaemia v0.132 HOXA11 Louise Daugherty Source Wessex and West Midlands GLH was added to HOXA11.
Source North West GLH was added to HOXA11.
Cytopenia - NOT Fanconi anaemia v0.132 GP9 Louise Daugherty gene: GP9 was added
gene: GP9 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: GP9 was set to
Cytopenia - NOT Fanconi anaemia v0.132 GP1BB Louise Daugherty gene: GP1BB was added
gene: GP1BB was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: GP1BB was set to
Cytopenia - NOT Fanconi anaemia v0.132 GP1BA Louise Daugherty Source Wessex and West Midlands GLH was added to GP1BA.
Source Yorkshire and North East GLH was added to GP1BA.
Source North West GLH was added to GP1BA.
Cytopenia - NOT Fanconi anaemia v0.132 GNE Louise Daugherty gene: GNE was added
gene: GNE was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: GNE was set to
Cytopenia - NOT Fanconi anaemia v0.132 GINS1 Louise Daugherty gene: GINS1 was added
gene: GINS1 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: GINS1 was set to
Cytopenia - NOT Fanconi anaemia v0.132 FYB1 Louise Daugherty Source Wessex and West Midlands GLH was added to FYB1.
Cytopenia - NOT Fanconi anaemia v0.132 FLNA Louise Daugherty gene: FLNA was added
gene: FLNA was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: FLNA was set to
Cytopenia - NOT Fanconi anaemia v0.132 FLI1 Louise Daugherty gene: FLI1 was added
gene: FLI1 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: FLI1 was set to
Cytopenia - NOT Fanconi anaemia v0.132 ETV6 Louise Daugherty Source Wessex and West Midlands GLH was added to ETV6.
Source North West GLH was added to ETV6.
Cytopenia - NOT Fanconi anaemia v0.132 DIAPH1 Louise Daugherty gene: DIAPH1 was added
gene: DIAPH1 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: DIAPH1 was set to
Cytopenia - NOT Fanconi anaemia v0.132 CYCS Louise Daugherty Source Wessex and West Midlands GLH was added to CYCS.
Source North West GLH was added to CYCS.
Cytopenia - NOT Fanconi anaemia v0.132 CLPB Louise Daugherty gene: CLPB was added
gene: CLPB was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: CLPB was set to
Cytopenia - NOT Fanconi anaemia v0.132 CDC42 Louise Daugherty gene: CDC42 was added
gene: CDC42 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: CDC42 was set to
Cytopenia - NOT Fanconi anaemia v0.132 CD40LG Louise Daugherty gene: CD40LG was added
gene: CD40LG was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: CD40LG was set to
Cytopenia - NOT Fanconi anaemia v0.132 CD40 Louise Daugherty gene: CD40 was added
gene: CD40 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: CD40 was set to
Cytopenia - NOT Fanconi anaemia v0.132 ARPC1B Louise Daugherty gene: ARPC1B was added
gene: ARPC1B was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: ARPC1B was set to
Cytopenia - NOT Fanconi anaemia v0.132 AP3B1 Louise Daugherty gene: AP3B1 was added
gene: AP3B1 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: AP3B1 was set to
Cytopenia - NOT Fanconi anaemia v0.132 ANKRD26 Louise Daugherty Source Wessex and West Midlands GLH was added to ANKRD26.
Source North West GLH was added to ANKRD26.
Cytopenia - NOT Fanconi anaemia v0.132 ADAMTS13 Louise Daugherty gene: ADAMTS13 was added
gene: ADAMTS13 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: ADAMTS13 was set to
Cytopenia - NOT Fanconi anaemia v0.132 ACTN1 Louise Daugherty gene: ACTN1 was added
gene: ACTN1 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: ACTN1 was set to
Cytopenia - NOT Fanconi anaemia v0.132 ACTB Louise Daugherty gene: ACTB was added
gene: ACTB was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: ACTB was set to
Cytopenia - NOT Fanconi anaemia v0.132 ABCG8 Louise Daugherty gene: ABCG8 was added
gene: ABCG8 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: ABCG8 was set to
Cytopenia - NOT Fanconi anaemia v0.132 ABCG5 Louise Daugherty gene: ABCG5 was added
gene: ABCG5 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH,Yorkshire and North East GLH,London South GLH,North West GLH,NHS GMS
Mode of inheritance for gene: ABCG5 was set to
Cytopenia - NOT Fanconi anaemia v0.131 TUBB1 Louise Daugherty Phenotypes for gene: TUBB1 were changed from 613112 Macrothrombocytopenia to Macrothrombocytopenia, 613112
Cytopenia - NOT Fanconi anaemia v0.130 STIM1 Louise Daugherty Phenotypes for gene: STIM1 were changed from 185070 Stormorken syndrome to Stormorken syndrome, 185070
Cytopenia - NOT Fanconi anaemia v0.129 SMARCAL1 Louise Daugherty Phenotypes for gene: SMARCAL1 were changed from 242900 Schimke immunoosseous dysplasia to Schimke immunoosseous dysplasia, 242900
Cytopenia - NOT Fanconi anaemia v0.128 SLC37A4 Louise Daugherty Phenotypes for gene: SLC37A4 were changed from 232220 Glycogen storage disease Ib to Glycogen storage disease Ib, 232220
Cytopenia - NOT Fanconi anaemia v0.127 RUNX1 Louise Daugherty Phenotypes for gene: RUNX1 were changed from 601399 Platelet disorder, familial, with associated myeloid malignancy to Platelet disorder, familial, with associated myeloid malignancy, 601399
Cytopenia - NOT Fanconi anaemia v0.126 NBEAL2 Louise Daugherty Phenotypes for gene: NBEAL2 were changed from 139090 Gray platelet syndrome to Gray platelet syndrome, 139090
Cytopenia - NOT Fanconi anaemia v0.125 MYH9 Louise Daugherty Phenotypes for gene: MYH9 were changed from 155100 Macrothrombocytopenia to Macrothrombocytopenia, 155100
Cytopenia - NOT Fanconi anaemia v0.124 HOXA11 Louise Daugherty Phenotypes for gene: HOXA11 were changed from 605432 Radioulnar synostosis with amegakaryocytic thrombocytopenia 1 to Radioulnar synostosis with amegakaryocytic thrombocytopenia 1, 605432
Cytopenia - NOT Fanconi anaemia v0.123 GP1BA Louise Daugherty Phenotypes for gene: GP1BA were changed from 231200 Bernard-Soulier syndrome, type A1 to Bernard-Soulier syndrome, type A1, 231200; Mild macrothrombocytopenia; Platelet type VWD, mild thrombocytopenia
Cytopenia - NOT Fanconi anaemia v0.122 CYCS Louise Daugherty Phenotypes for gene: CYCS were changed from 612004 Thrombocytopenia 4; Thrombocytopenia to Thrombocytopenia 4, 612004; Thrombocytopenia
Cytopenia - NOT Fanconi anaemia v0.121 ANKRD26 Louise Daugherty Phenotypes for gene: ANKRD26 were changed from 188000 Thrombocytopenia 2 to Thrombocytopenia 2, 188000
Cytopenia - NOT Fanconi anaemia v0.120 Louise Daugherty List of related panels changed from R91 to R91; R258
Cytopenia - NOT Fanconi anaemia v0.119 Louise Daugherty List of related panels changed from to R91
Cytopenia - NOT Fanconi anaemia v0.118 TP53 Louise Daugherty Classified gene: TP53 as Red List (low evidence)
Cytopenia - NOT Fanconi anaemia v0.118 TP53 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be downgraded from Green to Red. Noted by YNEGLH the gene is associated with breast cancer rather than cytopenia
Cytopenia - NOT Fanconi anaemia v0.118 TP53 Louise Daugherty Gene: tp53 has been classified as Red List (Low Evidence).
Cytopenia - NOT Fanconi anaemia v0.117 STIM1 Louise Daugherty Classified gene: STIM1 as Red List (low evidence)
Cytopenia - NOT Fanconi anaemia v0.117 STIM1 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be downgraded from Green to Red. Noted by YNEGLH as being Green on the Bleeding and Platelet disorders panel but should be Red on this panel
Cytopenia - NOT Fanconi anaemia v0.117 STIM1 Louise Daugherty Gene: stim1 has been classified as Red List (Low Evidence).
Cytopenia - NOT Fanconi anaemia v0.116 SMARCAL1 Louise Daugherty Classified gene: SMARCAL1 as Red List (low evidence)
Cytopenia - NOT Fanconi anaemia v0.116 SMARCAL1 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be downgraded from Green to Red. Noted by YNEGLH as syndromic
Cytopenia - NOT Fanconi anaemia v0.116 SMARCAL1 Louise Daugherty Gene: smarcal1 has been classified as Red List (Low Evidence).
Cytopenia - NOT Fanconi anaemia v0.115 SLC37A4 Louise Daugherty Classified gene: SLC37A4 as Red List (low evidence)
Cytopenia - NOT Fanconi anaemia v0.115 SLC37A4 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be downgraded from Green to Red. Noted by YNEGLH - other discipline (IEM-GSD) so should be Red on this panel
Cytopenia - NOT Fanconi anaemia v0.115 SLC37A4 Louise Daugherty Gene: slc37a4 has been classified as Red List (Low Evidence).
Cytopenia - NOT Fanconi anaemia v0.114 RUNX1 Louise Daugherty Classified gene: RUNX1 as Red List (low evidence)
Cytopenia - NOT Fanconi anaemia v0.114 RUNX1 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be downgraded from Green to Red. Noted by YNEGLH the gene is rated Green on the R90 Bleeding and platelet disorders panel and AML panel but should be Red for R91 Cytopenia - NOT Fanconi anaemia panel
Cytopenia - NOT Fanconi anaemia v0.114 RUNX1 Louise Daugherty Gene: runx1 has been classified as Red List (Low Evidence).
Cytopenia - NOT Fanconi anaemia v0.113 RPS27 Louise Daugherty Classified gene: RPS27 as Red List (low evidence)
Cytopenia - NOT Fanconi anaemia v0.113 RPS27 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be downgraded from Green to Red. Noted by YNEGLH the gene is rated Green on the R92 Rare anaemia panel but should be Red for R91 Cytopenia - NOT Fanconi anaemia panel
Cytopenia - NOT Fanconi anaemia v0.113 RPS27 Louise Daugherty Gene: rps27 has been classified as Red List (Low Evidence).
Cytopenia - NOT Fanconi anaemia v0.112 RPS27 Louise Daugherty Deleted their comment
Cytopenia - NOT Fanconi anaemia v0.112 NBEAL2 Louise Daugherty changed review comment from: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be downgraded from Green to Red.; to: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be downgraded from Green to Red. Noted by YNEGLH the gene is rated Green on the R90 Bleeding and platelet disorders panel but should be Red for R91 Cytopenia - NOT Fanconi anaemia panel
Cytopenia - NOT Fanconi anaemia v0.112 MYH9 Louise Daugherty changed review comment from: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be downgraded from Green to Red.; to: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be downgraded from Green to Red. Noted by YNEGLH the gene is rated Green on the R90 Bleeding and platelet disorders panel but should be Red for R91 Cytopenia - NOT Fanconi anaemia panel
Cytopenia - NOT Fanconi anaemia v0.112 NBEAL2 Louise Daugherty Classified gene: NBEAL2 as Red List (low evidence)
Cytopenia - NOT Fanconi anaemia v0.112 NBEAL2 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be downgraded from Green to Red.
Cytopenia - NOT Fanconi anaemia v0.112 NBEAL2 Louise Daugherty Gene: nbeal2 has been classified as Red List (Low Evidence).
Cytopenia - NOT Fanconi anaemia v0.111 MYH9 Louise Daugherty Classified gene: MYH9 as Red List (low evidence)
Cytopenia - NOT Fanconi anaemia v0.111 MYH9 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be downgraded from Green to Red.
Cytopenia - NOT Fanconi anaemia v0.111 MYH9 Louise Daugherty Gene: myh9 has been classified as Red List (Low Evidence).
Cytopenia - NOT Fanconi anaemia v0.110 LIG4 Louise Daugherty Classified gene: LIG4 as Red List (low evidence)
Cytopenia - NOT Fanconi anaemia v0.110 LIG4 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be downgraded from Green to Red. YNEGLH noted it was syndromic.
Cytopenia - NOT Fanconi anaemia v0.110 LIG4 Louise Daugherty Gene: lig4 has been classified as Red List (Low Evidence).
Cytopenia - NOT Fanconi anaemia v0.109 GP1BA Louise Daugherty Classified gene: GP1BA as Red List (low evidence)
Cytopenia - NOT Fanconi anaemia v0.109 GP1BA Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be downgraded from Green to Red. Noted by YNEGLH the gene is rated Green on the R90 Bleeding and platelet disorders panel but should be red for R91 Cytopenia - NOT Fanconi anaemia panel
Cytopenia - NOT Fanconi anaemia v0.109 GP1BA Louise Daugherty Gene: gp1ba has been classified as Red List (Low Evidence).
Cytopenia - NOT Fanconi anaemia v0.108 DDX41 Louise Daugherty Classified gene: DDX41 as Red List (low evidence)
Cytopenia - NOT Fanconi anaemia v0.108 DDX41 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be downgraded from Green to Red. YNEGLH noted this is a susceptibility gene.
Cytopenia - NOT Fanconi anaemia v0.108 DDX41 Louise Daugherty Gene: ddx41 has been classified as Red List (Low Evidence).
Cytopenia - NOT Fanconi anaemia v0.107 USB1 Louise Daugherty Mode of inheritance for gene: USB1 was changed from to BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.106 RPL31 Louise Daugherty Mode of inheritance for gene: RPL31 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Cytopenia - NOT Fanconi anaemia v0.105 RPL27 Louise Daugherty Mode of inheritance for gene: RPL27 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Cytopenia - NOT Fanconi anaemia v0.104 ADA2 Louise Daugherty Mode of inheritance for gene: ADA2 was changed from to BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.103 ADA2 Louise Daugherty Classified gene: ADA2 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.103 ADA2 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.103 ADA2 Louise Daugherty Gene: ada2 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.102 RPS7 Louise Daugherty Classified gene: RPS7 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.102 RPS7 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.102 RPS7 Louise Daugherty Gene: rps7 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.101 RPS27 Louise Daugherty Classified gene: RPS27 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.101 RPS27 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.101 RPS27 Louise Daugherty Gene: rps27 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.100 RPS26 Louise Daugherty Classified gene: RPS26 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.100 RPS26 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.100 RPS26 Louise Daugherty Gene: rps26 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.99 RPS24 Louise Daugherty Classified gene: RPS24 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.99 RPS24 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.99 RPS24 Louise Daugherty Gene: rps24 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.98 RPS19 Louise Daugherty Classified gene: RPS19 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.98 RPS19 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.98 RPS19 Louise Daugherty Gene: rps19 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.97 RPS17 Louise Daugherty Classified gene: RPS17 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.97 RPS17 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.97 RPS17 Louise Daugherty Gene: rps17 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.96 RPS10 Louise Daugherty Classified gene: RPS10 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.96 RPS10 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.96 RPS10 Louise Daugherty Gene: rps10 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.95 RPL9 Louise Daugherty Classified gene: RPL9 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.95 RPL9 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.95 RPL9 Louise Daugherty Gene: rpl9 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.94 RPL5 Louise Daugherty Classified gene: RPL5 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.94 RPL5 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.94 RPL5 Louise Daugherty Gene: rpl5 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.93 RPL35A Louise Daugherty Classified gene: RPL35A as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.93 RPL35A Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.93 RPL35A Louise Daugherty Gene: rpl35a has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.92 RPL31 Louise Daugherty Classified gene: RPL31 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.92 RPL31 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.92 RPL31 Louise Daugherty Gene: rpl31 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.91 RPS29 Louise Daugherty Classified gene: RPS29 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.91 RPS29 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.91 RPS29 Louise Daugherty Gene: rps29 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.90 RPL27 Louise Daugherty Classified gene: RPL27 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.90 RPL27 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.90 RPL27 Louise Daugherty Gene: rpl27 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.89 RPL26 Louise Daugherty Classified gene: RPL26 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.89 RPL26 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.89 RPL26 Louise Daugherty Gene: rpl26 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.88 RPL15 Louise Daugherty Classified gene: RPL15 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.88 RPL15 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.88 RPL15 Louise Daugherty Gene: rpl15 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.87 RPL11 Louise Daugherty Classified gene: RPL11 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.87 RPL11 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.87 RPL11 Louise Daugherty Gene: rpl11 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.86 WIPF1 Louise Daugherty Classified gene: WIPF1 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.86 WIPF1 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.86 WIPF1 Louise Daugherty Gene: wipf1 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.85 KLF1 Louise Daugherty Classified gene: KLF1 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.85 KLF1 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.85 KLF1 Louise Daugherty Gene: klf1 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.84 KIF23 Louise Daugherty Classified gene: KIF23 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.84 KIF23 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.84 KIF23 Louise Daugherty Gene: kif23 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.83 RMRP Louise Daugherty Classified gene: RMRP as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.83 RMRP Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.83 RMRP Louise Daugherty Gene: rmrp has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.82 ETV6 Louise Daugherty Classified gene: ETV6 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.82 ETV6 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.82 ETV6 Louise Daugherty Gene: etv6 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.81 ANKRD26 Louise Daugherty Classified gene: ANKRD26 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.81 ANKRD26 Louise Daugherty Added comment: Comment on list classification: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.81 ANKRD26 Louise Daugherty Gene: ankrd26 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.80 CYCS Louise Daugherty Classified gene: CYCS as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.80 CYCS Louise Daugherty Added comment: Comment on list classification: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.80 CYCS Louise Daugherty Gene: cycs has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.79 MPL Louise Daugherty Classified gene: MPL as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.79 MPL Louise Daugherty Added comment: Comment on list classification: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.79 MPL Louise Daugherty Gene: mpl has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.78 MECOM Louise Daugherty Classified gene: MECOM as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.78 MECOM Louise Daugherty Added comment: Comment on list classification: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.78 MECOM Louise Daugherty Gene: mecom has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.77 ACD Louise Daugherty changed review comment from: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that there is enough evidence to rate this gene Green.; to: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.77 PARN Louise Daugherty changed review comment from: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that there is enough evidence to rate this gene Green.; to: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that this gene should be in this panel and there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.77 PARN Louise Daugherty Classified gene: PARN as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.77 PARN Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.77 PARN Louise Daugherty Gene: parn has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.76 ACD Louise Daugherty Classified gene: ACD as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.76 ACD Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. Gene was not submitted by all GLHs so needed further review by all the GLHs. All agreed that there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.76 ACD Louise Daugherty Gene: acd has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.75 NOP10 Louise Daugherty changed review comment from: Discrepant reviews for NOP10. To be discussed at July workshop to agree rating

Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. All agreed that there is only enough evidence to rate this gene Amber.; to: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. All agreed that there is only enough evidence to rate this gene Amber.

Discrepant reviews for NOP10. To be discussed at July workshop to agree rating
Cytopenia - NOT Fanconi anaemia v0.75 NOP10 Louise Daugherty changed review comment from: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. All agreed that there is only enough evidence to rate this gene Amber.; to: Discrepant reviews for NOP10. To be discussed at July workshop to agree rating

Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. All agreed that there is only enough evidence to rate this gene Amber.
Cytopenia - NOT Fanconi anaemia v0.75 NOP10 Louise Daugherty Deleted their comment
Cytopenia - NOT Fanconi anaemia v0.75 NOP10 Louise Daugherty changed review comment from: Discrepant reviews for NOP10. To be discussed at July workshop to agree rating; to: Discrepant reviews for NOP10. To be discussed at July workshop to agree rating
Cytopenia - NOT Fanconi anaemia v0.75 NOP10 Louise Daugherty commented on gene: NOP10: Discrepant reviews for NOP10. To be discussed at July workshop to agree rating
Cytopenia - NOT Fanconi anaemia v0.75 NOP10 Louise Daugherty Classified gene: NOP10 as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.75 NOP10 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. All agreed that there is only enough evidence to rate this gene Amber.
Cytopenia - NOT Fanconi anaemia v0.75 NOP10 Louise Daugherty Gene: nop10 has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v0.74 NHP2 Louise Daugherty Classified gene: NHP2 as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.74 NHP2 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. All agreed that there is only enough evidence to rate this gene Amber.
Cytopenia - NOT Fanconi anaemia v0.74 NHP2 Louise Daugherty Gene: nhp2 has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v0.73 NHP2 Louise Daugherty commented on gene: NHP2: Discrepant reviews for NHP2. To be discussed at July workshop to agree rating
Cytopenia - NOT Fanconi anaemia v0.73 SRP72 Louise Daugherty Classified gene: SRP72 as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.73 SRP72 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. All agreed that there is only enough evidence to rate this gene Amber.
Cytopenia - NOT Fanconi anaemia v0.73 SRP72 Louise Daugherty Gene: srp72 has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v0.72 SRP72 Louise Daugherty commented on gene: SRP72: Discrepant reviews for SRP72. To be discussed at July workshop to agree rating
Cytopenia - NOT Fanconi anaemia v0.72 WRAP53 Louise Daugherty Classified gene: WRAP53 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.72 WRAP53 Louise Daugherty Added comment: Comment on list classification: Upgraded from Amber to Green. As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. All agreed that there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.72 WRAP53 Louise Daugherty Gene: wrap53 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.71 WRAP53 Louise Daugherty commented on gene: WRAP53: Discrepant reviews for WRAP53. Rated as Amber WWMGLH - Green rating LSGLH, YNEGLH, NWGLH. To be discussed at July workshop to agree rating
Cytopenia - NOT Fanconi anaemia v0.71 USB1 Louise Daugherty Classified gene: USB1 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.71 USB1 Louise Daugherty Added comment: Comment on list classification: Upgraded from Amber to Green. As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. All agreed that there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.71 USB1 Louise Daugherty Gene: usb1 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.70 USB1 Louise Daugherty commented on gene: USB1: Discrepant reviews for USB. Rated as Amber WWMGLH - Green rating LSGLH, YNEGLH, NWGLH. To be discussed at July workshop to agree rating
Cytopenia - NOT Fanconi anaemia v0.70 TINF2 Louise Daugherty Classified gene: TINF2 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.70 TINF2 Louise Daugherty Added comment: Comment on list classification: Upgraded from Amber to Green. As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. All agreed that there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.70 TINF2 Louise Daugherty Gene: tinf2 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.69 TINF2 Louise Daugherty commented on gene: TINF2: Discrepant reviews forTINF2. Rated as Amber WWMGLH - Green rating LSGLH, YNEGLH, NWGLH. To be discussed at July workshop to agree rating.
Cytopenia - NOT Fanconi anaemia v0.69 TERC Louise Daugherty Classified gene: TERC as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.69 TERC Louise Daugherty Added comment: Comment on list classification: Upgraded from Amber to Green. As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. All agreed that there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.69 TERC Louise Daugherty Gene: terc has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.68 TERC Louise Daugherty changed review comment from: RBM8A: Discrepant reviews for TERC. Rated as Amber WWMGLH - Green rating LSGLH, YNEGLH, NWGLH. To be discussed at July workshop to agree rating; to: Discrepant reviews for TERC. Rated as Amber WWMGLH - Green rating LSGLH, YNEGLH, NWGLH. To be discussed at July workshop to agree rating
Cytopenia - NOT Fanconi anaemia v0.68 TERC Louise Daugherty commented on gene: TERC: RBM8A: Discrepant reviews for TERC. Rated as Amber WWMGLH - Green rating LSGLH, YNEGLH, NWGLH. To be discussed at July workshop to agree rating
Cytopenia - NOT Fanconi anaemia v0.68 JAGN1 Louise Daugherty Classified gene: JAGN1 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.68 JAGN1 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. All agreed that there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.68 JAGN1 Louise Daugherty Gene: jagn1 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.67 RBM8A Louise Daugherty Classified gene: RBM8A as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.67 RBM8A Louise Daugherty Added comment: Comment on list classification: Downgraded from Green to Amber. As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. All agreed that there is only enough evidence to rate this gene Amber.
Cytopenia - NOT Fanconi anaemia v0.67 RBM8A Louise Daugherty Gene: rbm8a has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v0.66 RBM8A Louise Daugherty commented on gene: RBM8A: Discrepant reviews for RBM8A. Rated as Green by LSGLH, YNEGLH - Amber rating by NWGLH, no review WWMGLH. To be discussed at July workshop to agree rating
Cytopenia - NOT Fanconi anaemia v0.66 NBN Louise Daugherty changed review comment from: Discrepant reviews for NBN:Rated as Green by WWMGLH, NWGLH - Amber rating by YNEGLH, LSGLH. To be discussed at July workshop to agree rating.; to: Discrepant reviews for NBN:Rated as Green by WWMGLH, NWGLH - Amber rating by YNEGLH, LSGLH. To be discussed at July workshop to agree rating. As noted by LSGLH -not sure if this should be in Cytopenia panel – would this not be picked up on chromosome breakage? Then better to go for the single gene test R259.
Cytopenia - NOT Fanconi anaemia v0.66 NBN Louise Daugherty Classified gene: NBN as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.66 NBN Louise Daugherty Added comment: Comment on list classification: Downgraded from Green to Amber. As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. All agreed that there is only enough evidence to rate this gene Amber.
Cytopenia - NOT Fanconi anaemia v0.66 NBN Louise Daugherty Gene: nbn has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v0.65 NBN Louise Daugherty commented on gene: NBN: Discrepant reviews for NBN:Rated as Green by WWMGLH, NWGLH - Amber rating by YNEGLH, LSGLH. To be discussed at July workshop to agree rating.
Cytopenia - NOT Fanconi anaemia v0.65 JAGN1 Louise Daugherty commented on gene: JAGN1: Discrepant reviews for JAGN1 : 3 GLH GREEN, 1 GLH AMBER. To be discussed at July workshop to agree rating.
Cytopenia - NOT Fanconi anaemia v0.65 TERT Louise Daugherty Classified gene: TERT as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.65 TERT Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. All agreed that there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.65 TERT Louise Daugherty Gene: tert has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.64 TERT Louise Daugherty commented on gene: TERT: Discrepant reviews for TERT : 3 GLH GREEN, 1 GLH AMBER. To be discussed at July workshop to agree rating.
Cytopenia - NOT Fanconi anaemia v0.64 GATA2 Louise Daugherty Classified gene: GATA2 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.64 GATA2 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. All agreed that there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.64 GATA2 Louise Daugherty Gene: gata2 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.63 GATA2 Louise Daugherty commented on gene: GATA2: Discrepant reviews for GATA2 : 3 GLH GREEN, 1 GLH AMBER. To be discussed at July workshop to agree rating.
Cytopenia - NOT Fanconi anaemia v0.63 GATA1 Louise Daugherty Classified gene: GATA1 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.63 GATA1 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. All agreed that there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.63 GATA1 Louise Daugherty Gene: gata1 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.62 GATA1 Louise Daugherty commented on gene: GATA1: Discrepant reviews for GATA1 : 3 GLH GREEN, 1 GLH AMBER. To be discussed at July workshop to agree rating.
Cytopenia - NOT Fanconi anaemia v0.62 FYB1 Louise Daugherty Classified gene: FYB1 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.62 FYB1 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. All agreed that there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.62 FYB1 Louise Daugherty Gene: fyb1 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.61 FYB1 Louise Daugherty commented on gene: FYB1: Discrepant reviews for FYB1. Rated as Green by YNEGLH, LSGLH - Amber rating by NWGLH, no review by WWMGLH. To be discussed at July workshop to agree rating.
Cytopenia - NOT Fanconi anaemia v0.61 EFL1 Louise Daugherty changed review comment from: Discrepant reviews for EFL1: Rated as Green by LSGLH, YNEGLH- Amber rating NWGLH, no review by WWMGLH. To be discussed at July workshop to agree rating.; to: Discrepant reviews for EFL1: Rated as Green by LSGLH, YNEGLH- Amber rating NWGLH, no review by WWMGLH. To be discussed at July workshop to agree rating.
Cytopenia - NOT Fanconi anaemia v0.61 EFL1 Louise Daugherty Classified gene: EFL1 as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.61 EFL1 Louise Daugherty Added comment: Comment on list classification: Downgraded from Green to Amber. As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. All agreed that there is only enough evidence to rate this gene Amber.
Cytopenia - NOT Fanconi anaemia v0.61 EFL1 Louise Daugherty Gene: efl1 has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v0.60 EFL1 Louise Daugherty commented on gene: EFL1: Discrepant reviews for EFL1: Rated as Green by LSGLH, YNEGLH- Amber rating NWGLH, no review by WWMGLH. To be discussed at July workshop to agree rating.
Cytopenia - NOT Fanconi anaemia v0.60 CXCR4 Louise Daugherty Classified gene: CXCR4 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.60 CXCR4 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. All agreed that there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.60 CXCR4 Louise Daugherty Gene: cxcr4 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.59 CXCR4 Louise Daugherty commented on gene: CXCR4: Discrepant reviews for CXCR4 : 3 GLH GREEN, 1 GLH AMBER. To be discussed at July workshop to agree rating.
Cytopenia - NOT Fanconi anaemia v0.59 CTC1 Louise Daugherty Classified gene: CTC1 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.59 CTC1 Louise Daugherty Added comment: Comment on list classification: As discussed with the GMS Haematology Specialist Test Group at workshop 2nd July 2019. All agreed that there is enough evidence to rate this gene Green.
Cytopenia - NOT Fanconi anaemia v0.59 CTC1 Louise Daugherty Gene: ctc1 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.58 CTC1 Louise Daugherty commented on gene: CTC1: Discrepant reviews for CTC1 : 3 GLH GREEN, 1 GLH AMBER. To be discussed at July workshop to agree rating.
Cytopenia - NOT Fanconi anaemia v0.56 TUBB1 Louise Daugherty Classified gene: TUBB1 as Red List (low evidence)
Cytopenia - NOT Fanconi anaemia v0.56 TUBB1 Louise Daugherty Gene: tubb1 has been classified as Red List (Low Evidence).
Cytopenia - NOT Fanconi anaemia v0.55 TUBB1 Louise Daugherty Classified gene: TUBB1 as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.55 TUBB1 Louise Daugherty Gene: tubb1 has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v0.54 HOXA11 Louise Daugherty Classified gene: HOXA11 as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.54 HOXA11 Louise Daugherty Gene: hoxa11 has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v0.53 RPS29 Louise Daugherty Source London South GLH was added to RPS29.
Cytopenia - NOT Fanconi anaemia v0.53 RPS26 Louise Daugherty Source London South GLH was added to RPS26.
Cytopenia - NOT Fanconi anaemia v0.53 RPS24 Louise Daugherty Source London South GLH was added to RPS24.
Cytopenia - NOT Fanconi anaemia v0.53 RPS19 Louise Daugherty Source London South GLH was added to RPS19.
Cytopenia - NOT Fanconi anaemia v0.53 RPS7 Louise Daugherty Source London South GLH was added to RPS7.
Cytopenia - NOT Fanconi anaemia v0.53 RPL35A Louise Daugherty Source London South GLH was added to RPL35A.
Cytopenia - NOT Fanconi anaemia v0.53 RPL27 Louise Daugherty Source London South GLH was added to RPL27.
Cytopenia - NOT Fanconi anaemia v0.53 RPL26 Louise Daugherty Source London South GLH was added to RPL26.
Cytopenia - NOT Fanconi anaemia v0.53 RPL15 Louise Daugherty Source London South GLH was added to RPL15.
Cytopenia - NOT Fanconi anaemia v0.53 RPL11 Louise Daugherty Source London South GLH was added to RPL11.
Cytopenia - NOT Fanconi anaemia v0.53 RPS10 Louise Daugherty Source London South GLH was added to RPS10.
Cytopenia - NOT Fanconi anaemia v0.53 RPL9 Louise Daugherty Source London South GLH was added to RPL9.
Cytopenia - NOT Fanconi anaemia v0.53 RPL5 Louise Daugherty Source London South GLH was added to RPL5.
Cytopenia - NOT Fanconi anaemia v0.53 GATA1 Louise Daugherty Source London South GLH was added to GATA1.
Cytopenia - NOT Fanconi anaemia v0.53 CYCS Louise Daugherty Source London South GLH was added to CYCS.
Rating Changed from Green List (high evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.53 RPS17 Louise Daugherty Source London South GLH was added to RPS17.
Cytopenia - NOT Fanconi anaemia v0.53 RPL31 Louise Daugherty Source London South GLH was added to RPL31.
Cytopenia - NOT Fanconi anaemia v0.53 FYB1 Louise Daugherty Source London South GLH was added to FYB1.
Cytopenia - NOT Fanconi anaemia v0.52 RPS29 Louise Daugherty commented on gene: RPS29: New review/rating by Frances Smith, Viapath Kings College Hospital (Curation_Template_GMS_Haem_FS_updated_reviews_20190425.xlsx) on behalf of London South GLH for the GMS Haematology specialist test group. Gene rated as Green.
Cytopenia - NOT Fanconi anaemia v0.52 RPS26 Louise Daugherty commented on gene: RPS26: New review/rating by Frances Smith, Viapath Kings College Hospital (Curation_Template_GMS_Haem_FS_updated_reviews_20190425.xlsx) on behalf of London South GLH for the GMS Haematology specialist test group. Gene rated as Green.
Cytopenia - NOT Fanconi anaemia v0.52 RPS24 Louise Daugherty commented on gene: RPS24: New review/rating by Frances Smith, Viapath Kings College Hospital (Curation_Template_GMS_Haem_FS_updated_reviews_20190425.xlsx) on behalf of London South GLH for the GMS Haematology specialist test group. Gene rated as Green.
Cytopenia - NOT Fanconi anaemia v0.52 RPS19 Louise Daugherty commented on gene: RPS19: New review/rating by Frances Smith, Viapath Kings College Hospital (Curation_Template_GMS_Haem_FS_updated_reviews_20190425.xlsx) on behalf of London South GLH for the GMS Haematology specialist test group. Gene rated as Green.
Cytopenia - NOT Fanconi anaemia v0.52 RPS7 Louise Daugherty commented on gene: RPS7: New review/rating by Frances Smith, Viapath Kings College Hospital (Curation_Template_GMS_Haem_FS_updated_reviews_20190425.xlsx) on behalf of London South GLH for the GMS Haematology specialist test group. Gene rated as Green.
Cytopenia - NOT Fanconi anaemia v0.52 RPL35A Louise Daugherty commented on gene: RPL35A: New review/rating by Frances Smith, Viapath Kings College Hospital (Curation_Template_GMS_Haem_FS_updated_reviews_20190425.xlsx) on behalf of London South GLH for the GMS Haematology specialist test group. Gene rated as Green.
Cytopenia - NOT Fanconi anaemia v0.52 RPL27 Louise Daugherty commented on gene: RPL27: New review/rating by Frances Smith, Viapath Kings College Hospital (Curation_Template_GMS_Haem_FS_updated_reviews_20190425.xlsx) on behalf of London South GLH for the GMS Haematology specialist test group. Gene rated as Green.
Cytopenia - NOT Fanconi anaemia v0.52 RPL26 Louise Daugherty commented on gene: RPL26: New review/rating by Frances Smith, Viapath Kings College Hospital (Curation_Template_GMS_Haem_FS_updated_reviews_20190425.xlsx) on behalf of London South GLH for the GMS Haematology specialist test group. Gene rated as Green.
Cytopenia - NOT Fanconi anaemia v0.52 RPL15 Louise Daugherty commented on gene: RPL15: New review/rating by Frances Smith, Viapath Kings College Hospital (Curation_Template_GMS_Haem_FS_updated_reviews_20190425.xlsx) on behalf of London South GLH for the GMS Haematology specialist test group. Gene rated as Green.
Cytopenia - NOT Fanconi anaemia v0.52 RPL11 Louise Daugherty commented on gene: RPL11: New review/rating by Frances Smith, Viapath Kings College Hospital (Curation_Template_GMS_Haem_FS_updated_reviews_20190425.xlsx) on behalf of London South GLH for the GMS Haematology specialist test group. Gene rated as Green.
Cytopenia - NOT Fanconi anaemia v0.52 RPS10 Louise Daugherty commented on gene: RPS10: New review/rating by Frances Smith, Viapath Kings College Hospital (Curation_Template_GMS_Haem_FS_updated_reviews_20190425.xlsx) on behalf of London South GLH for the GMS Haematology specialist test group. Gene rated as Green.
Cytopenia - NOT Fanconi anaemia v0.52 RPL9 Louise Daugherty commented on gene: RPL9: New review/rating by Frances Smith, Viapath Kings College Hospital (Curation_Template_GMS_Haem_FS_updated_reviews_20190425.xlsx) on behalf of London South GLH for the GMS Haematology specialist test group. Gene rated as Green.
Cytopenia - NOT Fanconi anaemia v0.52 RPL5 Louise Daugherty commented on gene: RPL5: New review/rating by Frances Smith, Viapath Kings College Hospital (Curation_Template_GMS_Haem_FS_updated_reviews_20190425.xlsx) on behalf of London South GLH for the GMS Haematology specialist test group. Gene rated as Green.
Cytopenia - NOT Fanconi anaemia v0.52 GATA1 Louise Daugherty commented on gene: GATA1: New review/rating by Frances Smith, Viapath Kings College Hospital (Curation_Template_GMS_Haem_FS_updated_reviews_20190425.xlsx) on behalf of London South GLH for the GMS Haematology specialist test group. Gene rated as Green.
Cytopenia - NOT Fanconi anaemia v0.52 CYCS Louise Daugherty commented on gene: CYCS: New review/rating by Frances Smith, Viapath Kings College Hospital (Curation_Template_GMS_Haem_FS_updated_reviews_20190425.xlsx) on behalf of London South GLH for the GMS Haematology specialist test group. Gene rated as Green.
Cytopenia - NOT Fanconi anaemia v0.52 RPS17 Louise Daugherty commented on gene: RPS17: New review/rating by Frances Smith, Viapath Kings College Hospital (Curation_Template_GMS_Haem_FS_updated_reviews_20190425.xlsx) on behalf of London South GLH for the GMS Haematology specialist test group. Gene rated as Green.
Cytopenia - NOT Fanconi anaemia v0.52 RPL31 Louise Daugherty commented on gene: RPL31: New review/rating by Frances Smith, Viapath Kings College Hospital (Curation_Template_GMS_Haem_FS_updated_reviews_20190425.xlsx) on behalf of London South GLH for the GMS Haematology specialist test group. Gene rated as Green.
Cytopenia - NOT Fanconi anaemia v0.52 SAMD9L Louise Daugherty commented on gene: SAMD9L: Review/rating updated by Frances Smith, Viapath Kings College Hospital (Curation_Template_GMS_Haem_FS_updated_reviews_20190425.xlsx) from initial review February 2019, on behalf of London South GLH for the GMS Haematology specialist test group. Gene rating upgraded from Red to Green.
Cytopenia - NOT Fanconi anaemia v0.52 SAMD9 Louise Daugherty commented on gene: SAMD9: Review/rating updated by Frances Smith, Viapath Kings College Hospital (Curation_Template_GMS_Haem_FS_updated_reviews_20190425.xlsx) from initial review February 2019, on behalf of London South GLH for the GMS Haematology specialist test group. Gene rating upgraded from Red to Green.
Cytopenia - NOT Fanconi anaemia v0.52 GFI1 Louise Daugherty commented on gene: GFI1: Review/rating updated by Frances Smith, Viapath Kings College Hospital (Curation_Template_GMS_Haem_FS_updated_reviews_20190425.xlsx) from initial review February 2019, on behalf of London South GLH for the GMS Haematology specialist test group. Gene rating upgraded from Red to Green.
Cytopenia - NOT Fanconi anaemia v0.52 FYB1 Louise Daugherty commented on gene: FYB1: New review/rating by Frances Smith, Viapath Kings College Hospital (Curation_Template_GMS_Haem_FS_updated_reviews_20190425.xlsx) on behalf of London South GLH for the GMS Haematology specialist test group. Gene rated as Green.
Cytopenia - NOT Fanconi anaemia v0.51 RPS29 Frances Smith reviewed gene: RPS29: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.51 RPS26 Frances Smith reviewed gene: RPS26: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.51 RPS24 Frances Smith reviewed gene: RPS24: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.51 RPS19 Frances Smith reviewed gene: RPS19: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.51 RPS7 Frances Smith reviewed gene: RPS7: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.51 RPL35A Frances Smith reviewed gene: RPL35A: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.51 RPL27 Frances Smith reviewed gene: RPL27: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.51 RPL26 Frances Smith reviewed gene: RPL26: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.51 RPL15 Frances Smith reviewed gene: RPL15: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.51 RPL11 Frances Smith reviewed gene: RPL11: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.51 RPS10 Frances Smith reviewed gene: RPS10: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.51 RPL9 Frances Smith reviewed gene: RPL9: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.51 RPL5 Frances Smith reviewed gene: RPL5: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.51 GATA1 Frances Smith reviewed gene: GATA1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.51 CYCS Frances Smith reviewed gene: CYCS: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.51 RPS17 Frances Smith reviewed gene: RPS17: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.51 RPL31 Frances Smith reviewed gene: RPL31: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.51 SAMD9L Frances Smith edited their review of gene: SAMD9L: Changed rating: GREEN
Cytopenia - NOT Fanconi anaemia v0.51 SAMD9 Frances Smith edited their review of gene: SAMD9: Changed rating: GREEN
Cytopenia - NOT Fanconi anaemia v0.51 GFI1 Frances Smith edited their review of gene: GFI1: Changed rating: GREEN
Cytopenia - NOT Fanconi anaemia v0.51 FYB1 Frances Smith reviewed gene: FYB1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.50 RPL26 Louise Daugherty Phenotypes for gene: RPL26 were changed from ?Diamond-Blackfan anemia 11,614900 to ?Diamond-Blackfan anemia 11, 614900
Cytopenia - NOT Fanconi anaemia v0.49 RPL31 Louise Daugherty Phenotypes for gene: RPL31 were changed from to Diamond-Blackfan anaemia
Cytopenia - NOT Fanconi anaemia v0.48 RPS17 Louise Daugherty Publications for gene: RPS17 were set to 22045982; 19953637; 17647292; 19061985
Cytopenia - NOT Fanconi anaemia v0.47 CYCS Louise Daugherty Publications for gene: CYCS were set to
Cytopenia - NOT Fanconi anaemia v0.46 CYCS Louise Daugherty Phenotypes for gene: CYCS were changed from 612004 Thrombocytopenia 4 to 612004 Thrombocytopenia 4; Thrombocytopenia
Cytopenia - NOT Fanconi anaemia v0.45 GATA1 Louise Daugherty Publications for gene: GATA1 were set to 22706301; 24952648; 24766296; 10700180; 24453067
Cytopenia - NOT Fanconi anaemia v0.44 GATA1 Louise Daugherty Phenotypes for gene: GATA1 were changed from 314050 Thrombocytopenia with beta-thalassemia, X-linked; Diamond Blackfan Anaemia; Thrombocytopenia, X-linked, with or without dyserythropoietic anemia, 300367; Anemia, X-linked, with/without neutropenia and/or platelet abnormalities, 300835; Myelodysplastic syndrome (MDS), Paediatric to 314050 Thrombocytopenia with beta-thalassemia, X-linked; Diamond Blackfan Anaemia; Thrombocytopenia, X-linked, with or without dyserythropoietic anemia, 300367; Anemia, X-linked, with/without neutropenia and/or platelet abnormalities, 300835; Myelodysplastic syndrome (MDS), Paediatric; Anaemia; thrombocytopenia
Cytopenia - NOT Fanconi anaemia v0.43 RPL5 Louise Daugherty Phenotypes for gene: RPL5 were changed from Diamond-Blackfan anemia 6, 612561; DIAMOND-BLACKFAN ANEMIA 6; Diamond_Blackfan Anemia 6; Diamond-Blackfan Anemia; Inherited Bone Marrow Failure Syndromes; Diamond Blackfan anemia to Diamond-Blackfan anemia 6, 612561; DIAMOND-BLACKFAN ANEMIA 6; Diamond Blackfan Anemia 6; Diamond-Blackfan Anemia; Inherited Bone Marrow Failure Syndromes; Diamond Blackfan anemia
Cytopenia - NOT Fanconi anaemia v0.42 RPL9 Louise Daugherty Publications for gene: RPL9 were set to 23718193; 20116044
Cytopenia - NOT Fanconi anaemia v0.41 RPL11 Louise Daugherty Publications for gene: RPL11 were set to 19191325; 19061985
Cytopenia - NOT Fanconi anaemia v0.40 RPL15 Louise Daugherty Publications for gene: RPL15 were set to 23812780; 19438500
Cytopenia - NOT Fanconi anaemia v0.39 RPL35A Louise Daugherty Phenotypes for gene: RPL35A were changed from Diamond-Blackfan anemia 5, 612528; Diamond-Blackfan Anemia; DIAMOND-BLACKFAN ANEMIA 5; Inherited Bone Marrow Failure Syndromes; Diamond_Blackfan Anemia 5; Diamond Blackfan anemia to Diamond-Blackfan anemia 5, 612528; Diamond-Blackfan Anemia; DIAMOND-BLACKFAN ANEMIA 5; Inherited Bone Marrow Failure Syndromes; Diamond Blackfan Anemia 5; Diamond Blackfan anemia
Cytopenia - NOT Fanconi anaemia v0.38 RPS24 Louise Daugherty Publications for gene: RPS24 were set to 17186470; 19689926; 19773262; 25946618; 8647458; 2210388
Cytopenia - NOT Fanconi anaemia v0.37 RPS26 Louise Daugherty Publications for gene: RPS26 were set to 24675553; 25946618; 24942156; 20116044
Cytopenia - NOT Fanconi anaemia v0.36 RPS26 Louise Daugherty Phenotypes for gene: RPS26 were changed from Inherited Bone Marrow Failure Syndromes; Diamond_Blackfan Anemia 10; Diamond-Blackfan anemia 10; Diamond-Blackfan Anemia; Diamond-Blackfan anemia 10, 613309; Diamond Blackfan anemia to Inherited Bone Marrow Failure Syndromes; Diamond-Blackfan anemia 10; Diamond-Blackfan Anemia; Diamond-Blackfan anemia 10, 613309; Diamond Blackfan anemia
Cytopenia - NOT Fanconi anaemia v0.35 RPS29 Louise Daugherty Publications for gene: RPS29 were set to
Cytopenia - NOT Fanconi anaemia v0.34 RPS29 Louise Daugherty Phenotypes for gene: RPS29 were changed from Diamond-Blackfan anemia 13, 615909 to Diamond-Blackfan anemia 13, 615909; Diamond-Blackfan anaemia
Cytopenia - NOT Fanconi anaemia v0.33 RPS29 Louise Daugherty Phenotypes for gene: RPS29 were changed from Diamond-Blackfan anemia 13 615909 to Diamond-Blackfan anemia 13, 615909
Cytopenia - NOT Fanconi anaemia v0.32 PARN Louise Daugherty Phenotypes for gene: PARN were changed from 616371 Pulmonary fibrosis and/or bone marrow failure, telomere-related, 4; 616353 Dyskeratosis congenita, autosomal recessive 6,; 616353 Dyskeratosis congenita, autosomal recessive 6 to 616371 Pulmonary fibrosis and/or bone marrow failure, telomere-related, 4; 616353 Dyskeratosis congenita, autosomal recessive 6; 616353 Dyskeratosis congenita, autosomal recessive 6
Cytopenia - NOT Fanconi anaemia v0.31 PARN Mandy nesbitt edited their review of gene: PARN: Changed rating: GREEN; Changed phenotypes: 616371 Pulmonary fibrosis and/or bone marrow failure, telomere-related, 4, 616353 Dyskeratosis congenita, autosomal recessive 6
Cytopenia - NOT Fanconi anaemia v0.31 WRAP53 Louise Daugherty commented on gene: WRAP53: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: WRAP53; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: Inherited Bone Marrow Failure Syndromes;Dyskeratosis congenita;Dyskeratosis congenita, autosomal recessive 3, 613988;Dyskeratosis Congenita, Recessive;Dyskeratosis Congenita, Autosomal Recessive, 3; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.31 WIPF1 Louise Daugherty commented on gene: WIPF1: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: WIPF1; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: Wiskott-Aldrich syndrome like, WIP deficiency;WIP deficiency;?Wiskott-Aldrich syndrome 2 614493;Thrombocytopenia with or without small platelets, recurrent bacterial and viral infections, eczema, bloody diarrhea, WAS protein absent; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.31 WAS Louise Daugherty commented on gene: WAS: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: WAS; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females; Phenotypes: Neutropenia, severe congenital, X-linked 300299;Thrombocytopenia, X-linked 313900;Thrombocytopenia, X-linked, intermittent 313900;Wiskott-Aldrich syndrome 301000; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.31 VPS45 Louise Daugherty commented on gene: VPS45: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: VPS45; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: Neutropenia, severe congenital, 5, autosomal recessive, 615285;Congenital neutropenia-bone marrow fibrosis-nephromegaly syndrome;VPS45 deficiency;Severe congenital neutropenia; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.31 USB1 Louise Daugherty commented on gene: USB1: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: USB1; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: Poikiloderma with neutropenia 604173;Dyskeratosis congenita; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.31 TINF2 Louise Daugherty commented on gene: TINF2: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: TINF2; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown; Phenotypes: Inherited Bone Marrow Failure Syndromes;Inherited Bone Marrow Failure Syndromes - Aplastic Anaemia; Revesz Syndrome;Dyskeratosis congenita, autosomal dominant 3, 613990; Revesz syndrome, 268130;Revesz Syndrome;Dyskeratosis congenita;Dyskeratosis Congenita, Dominant;Dyskeratosis Congenita, Autosomal Dominant, 3;DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 3; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.31 THPO Louise Daugherty commented on gene: THPO: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: THPO; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Phenotypes: 187950 Thrombocythemia 1; PMID(s): 28466964; 24085763; 28559357; 29191945
Cytopenia - NOT Fanconi anaemia v0.31 TERT Louise Daugherty commented on gene: TERT: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: TERT; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Phenotypes: Aplastic Anemia;Coronary artery disease;{Dyskeratosis congenita, autosomal recessive 4}, 613989;{Dyskeratosis congenita, autosomal dominant 2}, 613989;{Pulmonary fibrosis, telomere-related, 1}, 614742;{Leukemia, acute myeloid}, 601626;{Melanoma, cutaneous malignant, 9}, 615134; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.31 TERC Louise Daugherty commented on gene: TERC: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: TERC; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown; Phenotypes: Inherited Bone Marrow Failure Syndromes;Inherited Bone Marrow Failure Syndromes - Aplastic Anaemia; Telomere_Related Pulmonary Fibrosis And/Or Bone Marrow Failure_2;Dyskeratosis congenita;Dyskeratosis Congenita, Autosomal Dominant, 1; Telomere_Related Pulmonary Fibrosis And/Or Bone Marrow Failure_1;DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.31 TAZ Louise Daugherty commented on gene: TAZ: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: TAZ; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females; Phenotypes: Barth syndrome 302060; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.31 SRP72 Louise Daugherty commented on gene: SRP72: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: SRP72; Suggested initial gene rating: I don't know; Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Phenotypes: Inherited Bone Marrow Failure Syndromes - Aplastic Anaemia; Bone Marrow Failure, Familial;Bone marrow failure, familial, 614675;Familial Bone Marrow Failure;Familial MDS (Myelodysplastic syndromes);Bone Marrow Failure, Familial; PMID(s): 22541560; 29146883
Cytopenia - NOT Fanconi anaemia v0.31 SBDS Louise Daugherty commented on gene: SBDS: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: SBDS; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: Shwachman-Diamond syndrome 260400; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.31 SAMD9L Louise Daugherty commented on gene: SAMD9L: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: SAMD9L; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown; Phenotypes: Ataxia-pancytopenia syndrome 159550; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.31 SAMD9 Louise Daugherty commented on gene: SAMD9: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: SAMD9; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown; Phenotypes: MIRAGE syndrome, 617053; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.31 RTEL1 Louise Daugherty commented on gene: RTEL1: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: RTEL1; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Phenotypes: Dyskeratosis congenita, autosomal recessive 5 615190;Dyskeratosis congenita, autosomal dominant 4 615190; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.31 RMRP Louise Daugherty commented on gene: RMRP: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: RMRP; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: Severe congenital neutropenia; Cartilage-hair hypoplasia; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.31 RBM8A Louise Daugherty commented on gene: RBM8A: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: RBM8A; Suggested initial gene rating: I don't know; Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Phenotypes: 616373 Pulmonary fibrosis and/or bone marrow failure, telomere-related; 615190 DC type 4 and 5; PMID(s): 22366785; 28128450; 24220582; 17236129
Cytopenia - NOT Fanconi anaemia v0.31 PARN Louise Daugherty commented on gene: PARN: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: PARN; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Phenotypes: 616371 Pulmonary fibrosis and/or bone marrow failure, telomere-related, 4; 616353 Dyskeratosis congenita, autosomal recessive 6; PMID(s): 25893599; 25848748; 26342108
Cytopenia - NOT Fanconi anaemia v0.31 NOP10 Louise Daugherty commented on gene: NOP10: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: NOP10; Suggested initial gene rating: I don't know; Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: Dyskeratosis congenita, autosomal recessive 1 224230; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.31 NHP2 Louise Daugherty commented on gene: NHP2: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: NHP2; Suggested initial gene rating: I don't know; Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: Dyskeratosis congenita, autosomal recessive 2 613987; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.31 MPL Louise Daugherty commented on gene: MPL: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: MPL; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Phenotypes: 604498 Thrombocytopenia, congenital amegakaryocytic; PMID(s): 10077649; 18024606
Cytopenia - NOT Fanconi anaemia v0.31 MPIG6B Louise Daugherty commented on gene: MPIG6B: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: MPIG6B; Suggested initial gene rating: I don't know; Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 61744 ?Thrombocytopenia, anemia, and myelofibrosis1; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.31 MECOM Louise Daugherty commented on gene: MECOM: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: MECOM; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Phenotypes: 616738 Radioulnar synostosis with amegakaryocytic thrombocytopenia 2; PMID(s): 29540340
Cytopenia - NOT Fanconi anaemia v0.31 LAT Louise Daugherty commented on gene: LAT: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: LAT; Suggested initial gene rating: I don't know; Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: Immunodeficiency 52, 617514; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.31 KLF1 Louise Daugherty commented on gene: KLF1: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: KLF1; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown; Phenotypes: Congenital Dyserythropoietic Anemia;Dyserythropoietic anemia, congenital, type IV, 613673; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.31 KIF23 Louise Daugherty commented on gene: KIF23: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: KIF23; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown; Phenotypes: Enzyme Disorder;Congenital dyserythropoietic anemia type III;CDA III;Congenital dyserythropoietic anemia (CDA); PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.31 JAGN1 Louise Daugherty commented on gene: JAGN1: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: JAGN1; Suggested initial gene rating: I don't know; Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 616022 Neutropenia, severe congenital, 6, autosomal recessive; PMID(s): 11101832
Cytopenia - NOT Fanconi anaemia v0.31 HAX1 Louise Daugherty commented on gene: HAX1: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: HAX1; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: Inherited Bone Marrow Failure Syndromes - Neutropenia;Severe congenital neutropenic;Neutropenia, Severe Congenital, 3 Autosomal Dominant;Neutropenia, severe congenital 3, autosomal recessive, 610738; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.31 GFI1 Louise Daugherty commented on gene: GFI1: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: GFI1; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Phenotypes: Inherited Bone Marrow Failure Syndromes - Neutropenia;Severe congenital neutropenic;Neutropenia, Severe Congenital, 2 Autosomal Dominant; Neutropenia, Nonimmune Chronic Idiopathic, Of Adults;Neutropenia, severe congenital 2, autosomal dominant, 613107; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.31 GATA2 Louise Daugherty commented on gene: GATA2: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: GATA2; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Phenotypes: Inherited Bone Marrow Failure Syndromes - GATA2 deficiencies;Familial MDS (Myelodysplastic syndromes);Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency, 614172;Emberger syndrome, 614038 (includes pancytopenia);{Myelodysplastic syndrome, susceptibility to}, 614286;{Leukemia, acute myeloid, susceptibility to}, 601626;Primary Lymphedema with Myelodysplasia;Immunodeficiency 21;Leukemia, Acute Myeloid;Lymphedema, Primary, With Myelodysplasia;Myelodysplastic Syndrome;Dendritic Cell, Monocyte, B Lymphocyte, And Natural Killer Lymphocyte Deficiency;Congenital dyserythropoietic anemia (CDA); PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.31 GATA1 Louise Daugherty commented on gene: GATA1: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: GATA1; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females; Phenotypes: Myelodysplastic syndrome (MDS), Paediatric;Diamond Blackfan Anaemia;Anemia, X-linked, with/without neutropenia and/or platelet abnormalities 300835;Thrombocytopenia, X-linked, with or without dyserythropoietic anemia 300367; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.31 G6PC3 Louise Daugherty commented on gene: G6PC3: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: G6PC3; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: Inherited Bone Marrow Failure Syndromes - Neutropenia;Severe congenital neutropenic;Neutropenia, Severe Congenital, 4 Autosomal Dominant;Neutropenia, severe congenital 4, autosomal recessive, 612541;Dursun syndrome, 612541;Severe Congenital Neutropenia; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.31 FYB1 Louise Daugherty commented on gene: FYB1: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: FYB1; Suggested initial gene rating: I don't know; Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 273900 Thrombocytopenia 3; PMID(s): 25876182; 25516138
Cytopenia - NOT Fanconi anaemia v0.31 ERCC6L2 Louise Daugherty commented on gene: ERCC6L2: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: ERCC6L2; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: Bone marrow failure syndrome 2, 615715; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.31 ELANE Louise Daugherty commented on gene: ELANE: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: ELANE; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown; Phenotypes: Neutropenia, cyclic 162800;Neutropenia, severe congenital 1, autosomal dominant 202700; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.31 EFL1 Louise Daugherty commented on gene: EFL1: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: EFL1; Suggested initial gene rating: I don't know; Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 617941 Shwachman-Diamond syndrome 2; PMID(s): 29970384, 28331068
Cytopenia - NOT Fanconi anaemia v0.31 DNAJC21 Louise Daugherty commented on gene: DNAJC21: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: DNAJC21; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: Pancytopaenia;Bone Marrow Failure;Bone marrow failure syndrome 3, 617052; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.31 DKC1 Louise Daugherty commented on gene: DKC1: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: DKC1; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females; Phenotypes: Dyskeratosis congenita;Dyskeratosis congenita, X-linked, 305000; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.31 CXCR4 Louise Daugherty commented on gene: CXCR4: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: CXCR4; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Phenotypes: WHIM syndrome, 193670;Warts, hypogammaglobulinemia, infections, and myelokathexis, Myelokathexis, isolated;Severe congenital neutropenia; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.31 CTC1 Louise Daugherty commented on gene: CTC1: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: CTC1; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: Inherited Bone Marrow Failure Syndromes;Dyskeratosis congenita;Dyskeratosis Congenita, Recessive;Cerebroretinal microangiopathy with calcifications and cysts/CTC1 related Dyskeratosis Congenita; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.31 CSF3R Louise Daugherty commented on gene: CSF3R: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: CSF3R; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: Severe congenital neutropenia;Neutropenia, severe congenital, 7, autosomal recessive 617014; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.31 ACD Louise Daugherty commented on gene: ACD: Initial gene list (Consensus Genes for SPEC HAEM Panels 31.01.19 North West v1 FINAL.xlsx) collated by Steve Keeney Molecular Diagnostics Centre Central Manchester NHS Foundation Trust January 2019 on behalf of North West GLH for the GMS Haematology specialist test group. Gene Symbol submitted: ACD; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Phenotypes: 616553 ?Dyskeratosis congenita 6 and 7; PMID(s): 25205116; 25233904
Cytopenia - NOT Fanconi anaemia v0.30 WRAP53 Steve Keeney reviewed gene: WRAP53: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Inherited Bone Marrow Failure Syndromes, Dyskeratosis congenita, Dyskeratosis congenita, autosomal recessive 3, 613988, Dyskeratosis Congenita, Recessive, Dyskeratosis Congenita, Autosomal Recessive, 3; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.30 WIPF1 Steve Keeney reviewed gene: WIPF1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Wiskott-Aldrich syndrome like, WIP deficiency, WIP deficiency, ?Wiskott-Aldrich syndrome 2, 614493, Thrombocytopenia with or without small platelets, recurrent bacterial and viral infections, eczema, bloody diarrhea, WAS protein absent; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.30 WAS Steve Keeney reviewed gene: WAS: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Neutropenia, severe congenital, X-linked, 300299, Thrombocytopenia, X-linked 313900, Thrombocytopenia, X-linked, intermittent 313900, Wiskott-Aldrich syndrome, 301000; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Cytopenia - NOT Fanconi anaemia v0.30 VPS45 Steve Keeney reviewed gene: VPS45: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Neutropenia, severe congenital, 5, autosomal recessive, 615285, Congenital neutropenia-bone marrow fibrosis-nephromegaly syndrome, VPS45 deficiency, Severe congenital neutropenia; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.30 USB1 Steve Keeney reviewed gene: USB1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Poikiloderma with neutropenia, 604173, Dyskeratosis congenita; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.30 TINF2 Steve Keeney reviewed gene: TINF2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Inherited Bone Marrow Failure Syndromes, Inherited Bone Marrow Failure Syndromes - Aplastic Anaemia, Revesz Syndrome, Dyskeratosis congenita, autosomal dominant 3, 613990, Revesz syndrome, 268130, Revesz Syndrome, Dyskeratosis congenita, Dyskeratosis Congenita, Dominant, Dyskeratosis Congenita, Autosomal Dominant, 3, DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 3; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Cytopenia - NOT Fanconi anaemia v0.30 THPO Steve Keeney reviewed gene: THPO: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Thrombocythemia 1, 187950; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v0.30 TERT Steve Keeney reviewed gene: TERT: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Aplastic Anemia, Coronary artery disease, {Dyskeratosis congenita, autosomal recessive 4}, 613989, {Dyskeratosis congenita, autosomal dominant 2}, 613989, {Pulmonary fibrosis, telomere-related, 1}, 614742, {Leukemia, acute myeloid}, 601626, {Melanoma, cutaneous malignant, 9}, 615134; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.30 TERC Steve Keeney reviewed gene: TERC: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Inherited Bone Marrow Failure Syndromes, Inherited Bone Marrow Failure Syndromes - Aplastic Anaemia, Telomere_Related Pulmonary Fibrosis And/Or Bone Marrow Failure_2, Dyskeratosis congenita, Dyskeratosis Congenita, Autosomal Dominant, 1, Telomere_Related Pulmonary Fibrosis And/Or Bone Marrow Failure_1, DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Cytopenia - NOT Fanconi anaemia v0.30 TAZ Steve Keeney reviewed gene: TAZ: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Barth syndrome, 302060; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Cytopenia - NOT Fanconi anaemia v0.30 SRP72 Steve Keeney reviewed gene: SRP72: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: Inherited Bone Marrow Failure Syndromes - Aplastic Anaemia, Bone Marrow Failure, Familial, Bone marrow failure, familial, 614675, Familial Bone Marrow Failure, Familial MDS (Myelodysplastic syndromes), Bone Marrow Failure, Familial; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v0.30 SBDS Steve Keeney reviewed gene: SBDS: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Shwachman-Diamond syndrome, 260400; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.30 SAMD9L Steve Keeney reviewed gene: SAMD9L: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Ataxia-pancytopenia syndrome, 159550; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Cytopenia - NOT Fanconi anaemia v0.30 SAMD9 Steve Keeney reviewed gene: SAMD9: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: MIRAGE syndrome, 617053; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Cytopenia - NOT Fanconi anaemia v0.30 RTEL1 Steve Keeney reviewed gene: RTEL1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Dyskeratosis congenita, autosomal recessive 5, 615190, Dyskeratosis congenita, autosomal dominant 4, 615190; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.30 RMRP Steve Keeney reviewed gene: RMRP: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Severe congenital neutropenia, Cartilage-hair hypoplasia; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.30 RBM8A Steve Keeney reviewed gene: RBM8A: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: 616373 Pulmonary fibrosis and/or bone marrow failure, telomere-related, 615190 DC type 4 and 5; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.30 PARN Steve Keeney reviewed gene: PARN: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 616371 Pulmonary fibrosis and/or bone marrow failure, telomere-related, 4, 616353 Dyskeratosis congenita, autosomal recessive 6; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.30 NOP10 Steve Keeney reviewed gene: NOP10: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: Dyskeratosis congenita, autosomal recessive 1, 224230; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.30 NHP2 Steve Keeney reviewed gene: NHP2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: Dyskeratosis congenita, autosomal recessive 2, 613987; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.30 MPL Steve Keeney reviewed gene: MPL: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Thrombocytopenia, congenital amegakaryocytic, 604498; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.30 MPIG6B Steve Keeney reviewed gene: MPIG6B: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ?Thrombocytopenia, anemia, and myelofibrosis1, 617441; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.30 MECOM Steve Keeney reviewed gene: MECOM: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Radioulnar synostosis with amegakaryocytic thrombocytopenia 2, 616738; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v0.30 LAT Steve Keeney reviewed gene: LAT: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: Immunodeficiency 52, 617514; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.30 KLF1 Steve Keeney reviewed gene: KLF1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Congenital Dyserythropoietic Anemia, Dyserythropoietic anemia, congenital, type IV, 613673; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Cytopenia - NOT Fanconi anaemia v0.30 KIF23 Steve Keeney reviewed gene: KIF23: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Enzyme Disorder, Congenital dyserythropoietic anemia type III, CDA III, Congenital dyserythropoietic anemia (CDA); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Cytopenia - NOT Fanconi anaemia v0.30 JAGN1 Steve Keeney reviewed gene: JAGN1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: 616022 Neutropenia, severe congenital, 6, autosomal recessive; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.30 HAX1 Steve Keeney reviewed gene: HAX1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Inherited Bone Marrow Failure Syndromes - Neutropenia, Severe congenital neutropenic, Neutropenia, Severe Congenital, 3 Autosomal Dominant, Neutropenia, severe congenital 3, autosomal recessive, 610738; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.30 GFI1 Steve Keeney reviewed gene: GFI1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Inherited Bone Marrow Failure Syndromes - Neutropenia, Severe congenital neutropenic, Neutropenia, Severe Congenital, 2 Autosomal Dominant, Neutropenia, Nonimmune Chronic Idiopathic, Of Adults, Neutropenia, severe congenital 2, autosomal dominant, 613107; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v0.30 GATA2 Steve Keeney reviewed gene: GATA2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Inherited Bone Marrow Failure Syndromes - GATA2 deficiencies, Familial MDS (Myelodysplastic syndromes), Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency, 614172, Emberger syndrome, 614038 (includes pancytopenia), {Myelodysplastic syndrome, susceptibility to}, 614286, {Leukemia, acute myeloid, susceptibility to}, 601626, Primary Lymphedema with Myelodysplasia, Immunodeficiency 21, Leukemia, Acute Myeloid, Lymphedema, Primary, With Myelodysplasia, Myelodysplastic Syndrome, Dendritic Cell, Monocyte, B Lymphocyte, And Natural Killer Lymphocyte Deficiency, Congenital dyserythropoietic anemia (CDA); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v0.30 GATA1 Steve Keeney reviewed gene: GATA1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Myelodysplastic syndrome (MDS), Paediatric, Diamond Blackfan Anaemia, Anemia, X-linked, with/without neutropenia and/or platelet abnormalities, 300835, Thrombocytopenia, X-linked, with or without dyserythropoietic anemia, 300367; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Cytopenia - NOT Fanconi anaemia v0.30 G6PC3 Steve Keeney reviewed gene: G6PC3: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Inherited Bone Marrow Failure Syndromes - Neutropenia, Severe congenital neutropenic, Neutropenia, Severe Congenital, 4 Autosomal Dominant, Neutropenia, severe congenital 4, autosomal recessive, 612541, Dursun syndrome, 612541, Severe Congenital Neutropenia; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.30 FYB1 Steve Keeney reviewed gene: FYB1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: Thrombocytopenia 3, 273900; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.30 ERCC6L2 Steve Keeney reviewed gene: ERCC6L2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Bone marrow failure syndrome 2, 615715; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.30 ELANE Steve Keeney reviewed gene: ELANE: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Neutropenia, cyclic, 162800, Neutropenia, severe congenital 1, autosomal dominant, 202700; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.30 EFL1 Steve Keeney reviewed gene: EFL1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: Shwachman-Diamond syndrome 2, 617941; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.30 DNAJC21 Steve Keeney reviewed gene: DNAJC21: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Pancytopaenia, Bone Marrow Failure, Bone marrow failure syndrome 3, 617052; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.30 DKC1 Steve Keeney reviewed gene: DKC1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Dyskeratosis congenita, Dyskeratosis congenita, X-linked, 305000; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Cytopenia - NOT Fanconi anaemia v0.30 CXCR4 Steve Keeney reviewed gene: CXCR4: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: WHIM syndrome, 193670, Warts, hypogammaglobulinemia, infections, and myelokathexis, Myelokathexis, isolated, Severe congenital neutropenia; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v0.30 CTC1 Steve Keeney reviewed gene: CTC1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Inherited Bone Marrow Failure Syndromes, Dyskeratosis congenita, Dyskeratosis Congenita, Recessive, Cerebroretinal microangiopathy with calcifications and cysts/CTC1 related Dyskeratosis Congenita; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.30 CSF3R Steve Keeney reviewed gene: CSF3R: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Severe congenital neutropenia, Neutropenia, severe congenital, 7, autosomal recessive, 617014; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.30 ACD Steve Keeney reviewed gene: ACD: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 616553 ?Dyskeratosis congenita 6 and 7; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.29 WRAP53 Louise Daugherty Added phenotypes Dyskeratosis Congenita, Autosomal Recessive, 3; Dyskeratosis Congenita, Recessive; Inherited Bone Marrow Failure Syndromes; Dyskeratosis congenita, autosomal recessive 3, 613988; Dyskeratosis congenita for gene: WRAP53
Cytopenia - NOT Fanconi anaemia v0.29 WIPF1 Louise Daugherty Added phenotypes WIP deficiency; Wiskott-Aldrich syndrome like, WIP deficiency; ?Wiskott-Aldrich syndrome 2, 614493; Thrombocytopenia with or without small platelets, recurrent bacterial and viral infections, eczema, bloody diarrhea, WAS protein absent for gene: WIPF1
Cytopenia - NOT Fanconi anaemia v0.29 WAS Louise Daugherty Added phenotypes Thrombocytopenia, X-linked, intermittent 313900; Thrombocytopenia, X-linked 313900; Wiskott-Aldrich syndrome, 301000; Neutropenia, severe congenital, X-linked, 300299 for gene: WAS
Cytopenia - NOT Fanconi anaemia v0.29 VPS45 Louise Daugherty Added phenotypes Congenital neutropenia-bone marrow fibrosis-nephromegaly syndrome; Neutropenia, severe congenital, 5, autosomal recessive, 615285; Severe congenital neutropenia; VPS45 deficiency for gene: VPS45
Cytopenia - NOT Fanconi anaemia v0.29 USB1 Louise Daugherty Added phenotypes Poikiloderma with neutropenia, 604173; Dyskeratosis congenita for gene: USB1
Cytopenia - NOT Fanconi anaemia v0.29 TINF2 Louise Daugherty Added phenotypes Inherited Bone Marrow Failure Syndromes - Aplastic Anaemia; Revesz Syndrome; Dyskeratosis Congenita, Autosomal Dominant, 3; DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 3; Dyskeratosis congenita; Dyskeratosis congenita, autosomal dominant 3, 613990; Revesz syndrome, 268130; Inherited Bone Marrow Failure Syndromes; Dyskeratosis Congenita, Dominant for gene: TINF2
Cytopenia - NOT Fanconi anaemia v0.29 THPO Louise Daugherty Added phenotypes Thrombocythemia 1, 187950 for gene: THPO
Publications for gene THPO were changed from 19553636; 10583217 to 24085763; 28466964; 28559357; 29191945
Cytopenia - NOT Fanconi anaemia v0.29 TERT Louise Daugherty Added phenotypes {Pulmonary fibrosis, telomere-related, 1}, 614742; {Dyskeratosis congenita, autosomal dominant 2}, 613989; Coronary artery disease; {Melanoma, cutaneous malignant, 9}, 615134; Aplastic Anemia; {Leukemia, acute myeloid}, 601626; {Dyskeratosis congenita, autosomal recessive 4}, 613989 for gene: TERT
Cytopenia - NOT Fanconi anaemia v0.29 TERC Louise Daugherty Added phenotypes Inherited Bone Marrow Failure Syndromes - Aplastic Anaemia; Telomere_Related Pulmonary Fibrosis And/Or Bone Marrow Failure_1; Telomere_Related Pulmonary Fibrosis And/Or Bone Marrow Failure_2; DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1; Dyskeratosis congenita; Dyskeratosis Congenita, Autosomal Dominant, 1; Inherited Bone Marrow Failure Syndromes for gene: TERC
Cytopenia - NOT Fanconi anaemia v0.29 TAZ Louise Daugherty Added phenotypes Barth syndrome, 302060 for gene: TAZ
Cytopenia - NOT Fanconi anaemia v0.29 SRP72 Louise Daugherty Added phenotypes Inherited Bone Marrow Failure Syndromes - Aplastic Anaemia; Familial Bone Marrow Failure; Bone Marrow Failure, Familial; Bone marrow failure, familial, 614675; Familial MDS (Myelodysplastic syndromes) for gene: SRP72
Publications for gene SRP72 were changed from 22541560 to 22541560; 29146883
Cytopenia - NOT Fanconi anaemia v0.29 SBDS Louise Daugherty Added phenotypes Shwachman-Diamond syndrome, 260400 for gene: SBDS
Cytopenia - NOT Fanconi anaemia v0.29 SAMD9L Louise Daugherty Added phenotypes Ataxia-pancytopenia syndrome, 159550 for gene: SAMD9L
Cytopenia - NOT Fanconi anaemia v0.29 SAMD9 Louise Daugherty Added phenotypes MIRAGE syndrome, 617053 for gene: SAMD9
Cytopenia - NOT Fanconi anaemia v0.29 RTEL1 Louise Daugherty Added phenotypes Dyskeratosis congenita, autosomal recessive 5, 615190; Dyskeratosis congenita, autosomal dominant 4, 615190 for gene: RTEL1
Cytopenia - NOT Fanconi anaemia v0.29 RMRP Louise Daugherty Added phenotypes Cartilage-hair hypoplasia; Severe congenital neutropenia for gene: RMRP
Cytopenia - NOT Fanconi anaemia v0.29 RBM8A Louise Daugherty Added phenotypes 616373 Pulmonary fibrosis and/or bone marrow failure, telomere-related; 615190 DC type 4 and 5 for gene: RBM8A
Publications for gene RBM8A were changed from 22366785; 17236129 to 22366785; 24220582; 28128450; 17236129
Cytopenia - NOT Fanconi anaemia v0.29 PARN Louise Daugherty Added phenotypes 616371 Pulmonary fibrosis and/or bone marrow failure, telomere-related, 4; 616353 Dyskeratosis congenita, autosomal recessive 6 for gene: PARN
Cytopenia - NOT Fanconi anaemia v0.29 NOP10 Louise Daugherty Added phenotypes Dyskeratosis congenita, autosomal recessive 1, 224230 for gene: NOP10
Cytopenia - NOT Fanconi anaemia v0.29 NHP2 Louise Daugherty Added phenotypes Dyskeratosis congenita, autosomal recessive 2, 613987 for gene: NHP2
Cytopenia - NOT Fanconi anaemia v0.29 MPL Louise Daugherty Added phenotypes Thrombocytopenia, congenital amegakaryocytic, 604498 for gene: MPL
Publications for gene MPL were changed from 11133753; 10077649 to 10077649; 18024606
Cytopenia - NOT Fanconi anaemia v0.29 MPIG6B Louise Daugherty Added phenotypes ?Thrombocytopenia, anemia, and myelofibrosis1, 617441 for gene: MPIG6B
Cytopenia - NOT Fanconi anaemia v0.29 MECOM Louise Daugherty Added phenotypes Radioulnar synostosis with amegakaryocytic thrombocytopenia 2, 616738 for gene: MECOM
Publications for gene MECOM were changed from 20091385; 26581901 to 29540340
Cytopenia - NOT Fanconi anaemia v0.29 LAT Louise Daugherty Added phenotypes Immunodeficiency 52, 617514 for gene: LAT
Cytopenia - NOT Fanconi anaemia v0.29 KLF1 Louise Daugherty Added phenotypes Dyserythropoietic anemia, congenital, type IV, 613673; Congenital Dyserythropoietic Anemia for gene: KLF1
Cytopenia - NOT Fanconi anaemia v0.29 KIF23 Louise Daugherty Added phenotypes CDA III; Congenital dyserythropoietic anemia (CDA); Congenital dyserythropoietic anemia type III; Enzyme Disorder for gene: KIF23
Cytopenia - NOT Fanconi anaemia v0.29 JAGN1 Louise Daugherty Added phenotypes 616022 Neutropenia, severe congenital, 6, autosomal recessive for gene: JAGN1
Publications for gene JAGN1 were changed from 25129144 to 11101832
Cytopenia - NOT Fanconi anaemia v0.29 HAX1 Louise Daugherty Added phenotypes Neutropenia, severe congenital 3, autosomal recessive, 610738; Inherited Bone Marrow Failure Syndromes - Neutropenia; Severe congenital neutropenic; Neutropenia, Severe Congenital, 3 Autosomal Dominant for gene: HAX1
Cytopenia - NOT Fanconi anaemia v0.29 GFI1 Louise Daugherty Added phenotypes Neutropenia, Nonimmune Chronic Idiopathic, Of Adults; Inherited Bone Marrow Failure Syndromes - Neutropenia; Neutropenia, Severe Congenital, 2 Autosomal Dominant; Severe congenital neutropenic; Neutropenia, severe congenital 2, autosomal dominant, 613107 for gene: GFI1
Cytopenia - NOT Fanconi anaemia v0.29 GATA2 Louise Daugherty Added phenotypes Congenital dyserythropoietic anemia (CDA); Myelodysplastic Syndrome; Familial MDS (Myelodysplastic syndromes); Leukemia, Acute Myeloid; {Leukemia, acute myeloid, susceptibility to}, 601626; Inherited Bone Marrow Failure Syndromes - GATA2 deficiencies; {Myelodysplastic syndrome, susceptibility to}, 614286; Primary Lymphedema with Myelodysplasia; Lymphedema, Primary, With Myelodysplasia; Dendritic Cell, Monocyte, B Lymphocyte, And Natural Killer Lymphocyte Deficiency; Immunodeficiency 21; Emberger syndrome, 614038 (includes pancytopenia); Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency, 614172 for gene: GATA2
Cytopenia - NOT Fanconi anaemia v0.29 GATA1 Louise Daugherty Added phenotypes Diamond Blackfan Anaemia; Thrombocytopenia, X-linked, with or without dyserythropoietic anemia, 300367; Anemia, X-linked, with/without neutropenia and/or platelet abnormalities, 300835; Myelodysplastic syndrome (MDS), Paediatric for gene: GATA1
Cytopenia - NOT Fanconi anaemia v0.29 G6PC3 Louise Daugherty Added phenotypes Dursun syndrome, 612541; Severe congenital neutropenic; Inherited Bone Marrow Failure Syndromes - Neutropenia; Neutropenia, severe congenital 4, autosomal recessive, 612541; Neutropenia, Severe Congenital, 4 Autosomal Dominant; Severe Congenital Neutropenia for gene: G6PC3
Cytopenia - NOT Fanconi anaemia v0.29 FYB1 Louise Daugherty Added phenotypes Thrombocytopenia 3, 273900 for gene: FYB1
Publications for gene FYB1 were changed from to 25516138; 25876182
Cytopenia - NOT Fanconi anaemia v0.29 ERCC6L2 Louise Daugherty Added phenotypes Bone marrow failure syndrome 2, 615715 for gene: ERCC6L2
Cytopenia - NOT Fanconi anaemia v0.29 ELANE Louise Daugherty Added phenotypes Neutropenia, severe congenital 1, autosomal dominant, 202700; Neutropenia, cyclic, 162800 for gene: ELANE
Cytopenia - NOT Fanconi anaemia v0.29 EFL1 Louise Daugherty Added phenotypes Shwachman-Diamond syndrome 2, 617941 for gene: EFL1
Publications for gene EFL1 were changed from 28331068 to 29970384, 28331068
Cytopenia - NOT Fanconi anaemia v0.29 DNAJC21 Louise Daugherty Added phenotypes Pancytopaenia; Bone Marrow Failure; Bone marrow failure syndrome 3, 617052 for gene: DNAJC21
Cytopenia - NOT Fanconi anaemia v0.29 DKC1 Louise Daugherty Added phenotypes Dyskeratosis congenita, X-linked, 305000; Dyskeratosis congenita for gene: DKC1
Cytopenia - NOT Fanconi anaemia v0.29 CXCR4 Louise Daugherty Added phenotypes Warts, hypogammaglobulinemia, infections, and myelokathexis, Myelokathexis, isolated; WHIM syndrome, 193670; Severe congenital neutropenia for gene: CXCR4
Cytopenia - NOT Fanconi anaemia v0.29 CTC1 Louise Daugherty Added phenotypes Cerebroretinal microangiopathy with calcifications and cysts/CTC1 related Dyskeratosis Congenita; Dyskeratosis Congenita, Recessive; Inherited Bone Marrow Failure Syndromes; Dyskeratosis congenita for gene: CTC1
Cytopenia - NOT Fanconi anaemia v0.29 CSF3R Louise Daugherty Added phenotypes Neutropenia, severe congenital, 7, autosomal recessive, 617014; Severe congenital neutropenia for gene: CSF3R
Cytopenia - NOT Fanconi anaemia v0.29 ACD Louise Daugherty Added phenotypes 616553 ?Dyskeratosis congenita 6 and 7 for gene: ACD
Cytopenia - NOT Fanconi anaemia v0.27 WRAP53 Louise Daugherty Source North West GLH was added to WRAP53.
Cytopenia - NOT Fanconi anaemia v0.27 WIPF1 Louise Daugherty Source North West GLH was added to WIPF1.
Cytopenia - NOT Fanconi anaemia v0.27 WAS Louise Daugherty Source North West GLH was added to WAS.
Cytopenia - NOT Fanconi anaemia v0.27 VPS45 Louise Daugherty Source North West GLH was added to VPS45.
Cytopenia - NOT Fanconi anaemia v0.27 USB1 Louise Daugherty Source North West GLH was added to USB1.
Cytopenia - NOT Fanconi anaemia v0.27 TINF2 Louise Daugherty Source North West GLH was added to TINF2.
Cytopenia - NOT Fanconi anaemia v0.27 THPO Louise Daugherty Source North West GLH was added to THPO.
Cytopenia - NOT Fanconi anaemia v0.27 TERT Louise Daugherty Source North West GLH was added to TERT.
Cytopenia - NOT Fanconi anaemia v0.27 TERC Louise Daugherty Source North West GLH was added to TERC.
Cytopenia - NOT Fanconi anaemia v0.27 TAZ Louise Daugherty Source North West GLH was added to TAZ.
Cytopenia - NOT Fanconi anaemia v0.27 SRP72 Louise Daugherty Source North West GLH was added to SRP72.
Cytopenia - NOT Fanconi anaemia v0.27 SBDS Louise Daugherty Source North West GLH was added to SBDS.
Cytopenia - NOT Fanconi anaemia v0.27 SAMD9L Louise Daugherty Source North West GLH was added to SAMD9L.
Cytopenia - NOT Fanconi anaemia v0.27 SAMD9 Louise Daugherty Source North West GLH was added to SAMD9.
Cytopenia - NOT Fanconi anaemia v0.27 RTEL1 Louise Daugherty Source North West GLH was added to RTEL1.
Cytopenia - NOT Fanconi anaemia v0.27 RMRP Louise Daugherty Source North West GLH was added to RMRP.
Cytopenia - NOT Fanconi anaemia v0.27 RBM8A Louise Daugherty Source North West GLH was added to RBM8A.
Cytopenia - NOT Fanconi anaemia v0.27 PARN Louise Daugherty Source North West GLH was added to PARN.
Cytopenia - NOT Fanconi anaemia v0.27 NOP10 Louise Daugherty Source North West GLH was added to NOP10.
Cytopenia - NOT Fanconi anaemia v0.27 NHP2 Louise Daugherty Source North West GLH was added to NHP2.
Cytopenia - NOT Fanconi anaemia v0.27 MPL Louise Daugherty Source North West GLH was added to MPL.
Cytopenia - NOT Fanconi anaemia v0.27 MPIG6B Louise Daugherty Source North West GLH was added to MPIG6B.
Cytopenia - NOT Fanconi anaemia v0.27 MECOM Louise Daugherty Source North West GLH was added to MECOM.
Cytopenia - NOT Fanconi anaemia v0.27 LAT Louise Daugherty Source North West GLH was added to LAT.
Cytopenia - NOT Fanconi anaemia v0.27 KLF1 Louise Daugherty Source North West GLH was added to KLF1.
Cytopenia - NOT Fanconi anaemia v0.27 KIF23 Louise Daugherty Source North West GLH was added to KIF23.
Cytopenia - NOT Fanconi anaemia v0.27 JAGN1 Louise Daugherty Source North West GLH was added to JAGN1.
Cytopenia - NOT Fanconi anaemia v0.27 HAX1 Louise Daugherty Source North West GLH was added to HAX1.
Cytopenia - NOT Fanconi anaemia v0.27 GFI1 Louise Daugherty Source North West GLH was added to GFI1.
Cytopenia - NOT Fanconi anaemia v0.27 GATA2 Louise Daugherty Source North West GLH was added to GATA2.
Cytopenia - NOT Fanconi anaemia v0.27 GATA1 Louise Daugherty Source North West GLH was added to GATA1.
Cytopenia - NOT Fanconi anaemia v0.27 G6PC3 Louise Daugherty Source North West GLH was added to G6PC3.
Cytopenia - NOT Fanconi anaemia v0.27 FYB1 Louise Daugherty Source North West GLH was added to FYB1.
Rating Changed from Green List (high evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.27 ERCC6L2 Louise Daugherty Source North West GLH was added to ERCC6L2.
Cytopenia - NOT Fanconi anaemia v0.27 ELANE Louise Daugherty Source North West GLH was added to ELANE.
Cytopenia - NOT Fanconi anaemia v0.27 EFL1 Louise Daugherty Source North West GLH was added to EFL1.
Cytopenia - NOT Fanconi anaemia v0.27 DNAJC21 Louise Daugherty Source North West GLH was added to DNAJC21.
Cytopenia - NOT Fanconi anaemia v0.27 DKC1 Louise Daugherty Source North West GLH was added to DKC1.
Cytopenia - NOT Fanconi anaemia v0.27 CXCR4 Louise Daugherty Source North West GLH was added to CXCR4.
Cytopenia - NOT Fanconi anaemia v0.27 CTC1 Louise Daugherty Source North West GLH was added to CTC1.
Cytopenia - NOT Fanconi anaemia v0.27 CSF3R Louise Daugherty Source North West GLH was added to CSF3R.
Cytopenia - NOT Fanconi anaemia v0.27 ACD Louise Daugherty Source North West GLH was added to ACD.
Cytopenia - NOT Fanconi anaemia v0.26 TP53 Louise Daugherty Mode of inheritance for gene: TP53 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v0.25 TP53 Louise Daugherty Classified gene: TP53 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.25 TP53 Louise Daugherty Gene: tp53 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.24 MYSM1 Louise Daugherty Mode of inheritance for gene: MYSM1 was changed from to BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.23 MYSM1 Louise Daugherty Classified gene: MYSM1 as Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.23 MYSM1 Louise Daugherty Gene: mysm1 has been classified as Amber List (Moderate Evidence).
Cytopenia - NOT Fanconi anaemia v0.22 FYB1 Louise Daugherty Mode of inheritance for gene: FYB1 was changed from to BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.21 FYB1 Louise Daugherty Classified gene: FYB1 as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.21 FYB1 Louise Daugherty Gene: fyb1 has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.20 CYCS Louise Daugherty Mode of inheritance for gene: CYCS was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v0.19 CYCS Louise Daugherty Classified gene: CYCS as Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.19 CYCS Louise Daugherty Gene: cycs has been classified as Green List (High Evidence).
Cytopenia - NOT Fanconi anaemia v0.18 WRAP53 Louise Daugherty commented on gene: WRAP53: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: WRAP53; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 300299 Neutropenia, severe congenital, X-linked; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 WAS Louise Daugherty commented on gene: WAS: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: WAS; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females; Phenotypes: 313900 Thrombocytopenia, X-linked; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 VPS45 Louise Daugherty commented on gene: VPS45: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: VPS45; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 615285 Neutropenia, severe congenital, 5, autosomal recessive; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 USB1 Louise Daugherty commented on gene: USB1: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: USB1; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 604173 Poikiloderma with neutropenia; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 TP53 Louise Daugherty reviewed gene: TP53: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.18 TINF2 Louise Daugherty commented on gene: TINF2: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: TINF2; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Phenotypes: 613990 Dyskeratosis congenita, autosomal dominant 3; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 THPO Louise Daugherty commented on gene: THPO: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: THPO; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Phenotypes: 187950 Thrombocythemia 1; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 TERT Louise Daugherty commented on gene: TERT: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: TERT; Suggested initial gene rating: I don't know; Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Phenotypes: 614742 {Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1}; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 TERC Louise Daugherty commented on gene: TERC: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: TERC; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Phenotypes: 614743 pulmonary fibrosis and/or bone marrow failure; 129550 Dyskeratosis congenita, autosomal dominant 1; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 TAZ Louise Daugherty commented on gene: TAZ: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: TAZ; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females; Phenotypes: 302060 Barth syndrome; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 SRP72 Louise Daugherty commented on gene: SRP72: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: SRP72; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Phenotypes: 614675 Bone marrow failure syndrome 1; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 SBDS Louise Daugherty commented on gene: SBDS: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: SBDS; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 260400 Shwachman-Diamond syndrome; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 SAMD9L Louise Daugherty commented on gene: SAMD9L: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: SAMD9L; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Phenotypes: 159550 Ataxia-pancytopenia syndrome; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 SAMD9 Louise Daugherty commented on gene: SAMD9: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: SAMD9; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Phenotypes: 617053 MIRAGE syndrome; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 RTEL1 Louise Daugherty commented on gene: RTEL1: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: RTEL1; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Phenotypes: 616373 Pulmonary fibrosis and/or bone marrow failure, telomere-related; 615190 DC type 4 and 5; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 RBM8A Louise Daugherty commented on gene: RBM8A: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: RBM8A; Suggested initial gene rating: I don't know; Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 274000 Thrombocytopenia-absent radius syndrome; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 PARN Louise Daugherty commented on gene: PARN: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: PARN; Suggested initial gene rating: not submitted ; Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Phenotypes: 616371 Pulmonary fibrosis and/or bone marrow failure, telomere-related, 4; 616353 Dyskeratosis congenita, autosomal recessive 6; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 NBN Louise Daugherty commented on gene: NBN: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: NBN; Suggested initial gene rating: not submitted ; Are variants in this gene part of your current diagnostic practice? info not submitted; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 251260 Nijmegen breakage syndrome; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 MYSM1 Louise Daugherty reviewed gene: MYSM1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.18 MPL Louise Daugherty commented on gene: MPL: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: MPL; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Phenotypes: 604498 Thrombocytopenia, congenital amegakaryocytic; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 MECOM Louise Daugherty commented on gene: MECOM: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: MECOM; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Phenotypes: 616738 Radioulnar synostosis with amegakaryocytic thrombocytopenia 2; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 JAGN1 Louise Daugherty commented on gene: JAGN1: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: JAGN1; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 616022 Neutropenia, severe congenital, 6, autosomal recessive; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 HOXA11 Louise Daugherty commented on gene: HOXA11: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: HOXA11; Suggested initial gene rating: I don't know; Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Phenotypes: 605432 Radioulnar synostosis with amegakaryocytic thrombocytopenia 1; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 HAX1 Louise Daugherty commented on gene: HAX1: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: HAX1; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 610738 Neutropenia, severe congenital 3, autosomal recessive; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 GFI1 Louise Daugherty commented on gene: GFI1: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: GFI1; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Phenotypes: 607847 ?Neutropenia, nonimmune chronic idiopathic, of adults; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 GATA2 Louise Daugherty commented on gene: GATA2: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: GATA2; Suggested initial gene rating: I don't know; Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Phenotypes: 614038 Emberger syndrome; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 GATA1 Louise Daugherty commented on gene: GATA1: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: GATA1; Suggested initial gene rating: I don't know; Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females; Phenotypes: 314050 Thrombocytopenia with beta-thalassemia, X-linked; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 G6PC3 Louise Daugherty commented on gene: G6PC3: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: G6PC3; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 612541 Neutropenia, severe congenital 4, autosomal recessive; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 FYB1 Louise Daugherty reviewed gene: FYB1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.18 ETV6 Louise Daugherty commented on gene: ETV6: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: ETV6; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Phenotypes: 616216 Thrombocytopenia 5; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 ERCC6L2 Louise Daugherty commented on gene: ERCC6L2: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: ERCC6L2; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 615715 Bone marrow failure syndrome 2; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 ELANE Louise Daugherty commented on gene: ELANE: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: ELANE; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Phenotypes: 202700 Neutropenia, severe congenital 1, autosomal dominant; 162800 Neutropenia, cyclic; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 EFL1 Louise Daugherty commented on gene: EFL1: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: EFL1; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 617941 Shwachman-Diamond syndrome 2; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 DNAJC21 Louise Daugherty commented on gene: DNAJC21: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: DNAJC21; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 617052 Bone marrow failure syndrome 3; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 DKC1 Louise Daugherty commented on gene: DKC1: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: DKC1; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females; Phenotypes: 305000 Dyskeratosis congenita; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 CYCS Louise Daugherty reviewed gene: CYCS: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.18 CXCR4 Louise Daugherty commented on gene: CXCR4: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: CXCR4; Suggested initial gene rating: I don't know; Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Phenotypes: 193670 WHIM syndrome; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 CTC1 Louise Daugherty commented on gene: CTC1: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: CTC1; Suggested initial gene rating: I don't know; Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: N/A Dyskeratosis congenita; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 CSF3R Louise Daugherty commented on gene: CSF3R: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: CSF3R; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 617014 Neutropenia, severe congenital, 7, autosomal recessive; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 ANKRD26 Louise Daugherty commented on gene: ANKRD26: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: ANKRD26; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Phenotypes: 188000 Thrombocytopenia 2; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.18 ACD Louise Daugherty commented on gene: ACD: Initial gene list (Consensus Genes for Panels_Haem_SHEFFIELD-29.01.2019.xlsx) collated by Mandy Nesbitt Sheffield Diagnostic Genetics Service, Sheffield Children's NHS Trust January 2019 on behalf of Yorkshire and North East GLH for the GMS Haematology specialist test group. Gene Symbol submitted: ACD; Suggested initial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Phenotypes: 616553 ?Dyskeratosis congenita 6 and 7; PMID(s): none submitted
Cytopenia - NOT Fanconi anaemia v0.17 WRAP53 Mandy nesbitt reviewed gene: WRAP53: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 300299 Neutropenia, severe congenital, X-linked; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.17 WAS Mandy nesbitt reviewed gene: WAS: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 313900 Thrombocytopenia, X-linked; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.17 VPS45 Mandy nesbitt reviewed gene: VPS45: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 615285 Neutropenia, severe congenital, 5, autosomal recessive; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.17 USB1 Mandy nesbitt reviewed gene: USB1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 604173 Poikiloderma with neutropenia; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.17 TP53 Mandy nesbitt reviewed gene: TP53: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 618165 Bone marrow failure syndrome 5; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v0.17 TINF2 Mandy nesbitt reviewed gene: TINF2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 613990 Dyskeratosis congenita, autosomal dominant 3; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.17 THPO Mandy nesbitt reviewed gene: THPO: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 187950 Thrombocythemia 1; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v0.17 TERT Mandy nesbitt reviewed gene: TERT: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: 614742 {Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1}; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.17 TERC Mandy nesbitt reviewed gene: TERC: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 614743 pulmonary fibrosis and/or bone marrow failure, 129550 Dyskeratosis congenita, autosomal dominant 1; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.17 TAZ Mandy nesbitt reviewed gene: TAZ: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 302060 Barth syndrome; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Cytopenia - NOT Fanconi anaemia v0.17 SRP72 Mandy nesbitt reviewed gene: SRP72: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 614675 Bone marrow failure syndrome 1; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.17 SBDS Mandy nesbitt reviewed gene: SBDS: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 260400 Shwachman-Diamond syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.17 SAMD9L Mandy nesbitt reviewed gene: SAMD9L: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 159550 Ataxia-pancytopenia syndrome; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v0.17 SAMD9 Mandy nesbitt reviewed gene: SAMD9: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 617053 MIRAGE syndrome; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v0.17 RTEL1 Mandy nesbitt reviewed gene: RTEL1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 616373 Pulmonary fibrosis and/or bone marrow failure, telomere-related, 615190 DC type 4 and 5; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.17 RBM8A Mandy nesbitt reviewed gene: RBM8A: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: 274000 Thrombocytopenia-absent radius syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.17 PARN Mandy nesbitt reviewed gene: PARN: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: 616371 Pulmonary fibrosis and/or bone marrow failure, telomere-related, 4, 616353 Dyskeratosis congenita, autosomal recessive 6; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.17 NBN Mandy nesbitt reviewed gene: NBN: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: 251260 Nijmegen breakage syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.17 MYSM1 Mandy nesbitt reviewed gene: MYSM1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: 618116 Bone marrow failure syndrome 4; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.17 MPL Mandy nesbitt reviewed gene: MPL: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 604498 Thrombocytopenia, congenital amegakaryocytic; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.17 MECOM Mandy nesbitt reviewed gene: MECOM: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 616738 Radioulnar synostosis with amegakaryocytic thrombocytopenia 2; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v0.17 JAGN1 Mandy nesbitt reviewed gene: JAGN1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 616022 Neutropenia, severe congenital, 6, autosomal recessive; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.17 HOXA11 Mandy nesbitt reviewed gene: HOXA11: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: 605432 Radioulnar synostosis with amegakaryocytic thrombocytopenia 1; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v0.17 HAX1 Mandy nesbitt reviewed gene: HAX1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 610738 Neutropenia, severe congenital 3, autosomal recessive; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.17 GFI1 Mandy nesbitt reviewed gene: GFI1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 607847 ?Neutropenia, nonimmune chronic idiopathic, of adults; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.17 GATA2 Mandy nesbitt reviewed gene: GATA2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: 614038 Emberger syndrome; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.17 GATA1 Mandy nesbitt reviewed gene: GATA1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: 314050 Thrombocytopenia with beta-thalassemia, X-linked; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.17 G6PC3 Mandy nesbitt reviewed gene: G6PC3: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 612541 Neutropenia, severe congenital 4, autosomal recessive; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.17 FYB1 Mandy nesbitt reviewed gene: FYB1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 273900 Thrombocytopenia 3; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.17 ETV6 Mandy nesbitt reviewed gene: ETV6: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 616216 Thrombocytopenia 5; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v0.17 ERCC6L2 Mandy nesbitt reviewed gene: ERCC6L2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 615715 Bone marrow failure syndrome 2; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.17 ELANE Mandy nesbitt reviewed gene: ELANE: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 202700 Neutropenia, severe congenital 1, autosomal dominant, 162800 Neutropenia, cyclic; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.17 EFL1 Mandy nesbitt reviewed gene: EFL1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 617941 Shwachman-Diamond syndrome 2; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.17 DNAJC21 Mandy nesbitt reviewed gene: DNAJC21: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 617052 Bone marrow failure syndrome 3; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.17 DKC1 Mandy nesbitt reviewed gene: DKC1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 305000 Dyskeratosis congenita; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females
Cytopenia - NOT Fanconi anaemia v0.17 CYCS Mandy nesbitt reviewed gene: CYCS: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 612004 Thrombocytopenia 4; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v0.17 CXCR4 Mandy nesbitt reviewed gene: CXCR4: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: 193670 WHIM syndrome; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v0.17 CTC1 Mandy nesbitt reviewed gene: CTC1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: Dyskeratosis congenita; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.17 CSF3R Mandy nesbitt reviewed gene: CSF3R: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 617014 Neutropenia, severe congenital, 7, autosomal recessive; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.17 ANKRD26 Mandy nesbitt reviewed gene: ANKRD26: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 188000 Thrombocytopenia 2; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v0.17 ACD Mandy nesbitt reviewed gene: ACD: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 616553 ?Dyskeratosis congenita 6 and 7; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.16 WRAP53 Louise Daugherty Added phenotypes 300299 Neutropenia, severe congenital, X-linked for gene: WRAP53
Cytopenia - NOT Fanconi anaemia v0.16 WAS Louise Daugherty Added phenotypes 313900 Thrombocytopenia, X-linked for gene: WAS
Cytopenia - NOT Fanconi anaemia v0.16 VPS45 Louise Daugherty Added phenotypes 615285 Neutropenia, severe congenital, 5, autosomal recessive for gene: VPS45
Cytopenia - NOT Fanconi anaemia v0.16 USB1 Louise Daugherty Added phenotypes 604173 Poikiloderma with neutropenia for gene: USB1
Cytopenia - NOT Fanconi anaemia v0.16 TP53 Louise Daugherty Added phenotypes 618165 Bone marrow failure syndrome 5 for gene: TP53
Cytopenia - NOT Fanconi anaemia v0.16 TINF2 Louise Daugherty Added phenotypes 613990 Dyskeratosis congenita, autosomal dominant 3 for gene: TINF2
Cytopenia - NOT Fanconi anaemia v0.16 THPO Louise Daugherty Added phenotypes 187950 Thrombocythemia 1 for gene: THPO
Cytopenia - NOT Fanconi anaemia v0.16 TERT Louise Daugherty Added phenotypes 614742 {Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1} for gene: TERT
Cytopenia - NOT Fanconi anaemia v0.16 TERC Louise Daugherty Added phenotypes 614743 pulmonary fibrosis and/or bone marrow failure; 129550 Dyskeratosis congenita, autosomal dominant 1 for gene: TERC
Cytopenia - NOT Fanconi anaemia v0.16 TAZ Louise Daugherty Added phenotypes 302060 Barth syndrome for gene: TAZ
Cytopenia - NOT Fanconi anaemia v0.16 SRP72 Louise Daugherty Added phenotypes 614675 Bone marrow failure syndrome 1 for gene: SRP72
Cytopenia - NOT Fanconi anaemia v0.16 SBDS Louise Daugherty Added phenotypes 260400 Shwachman-Diamond syndrome for gene: SBDS
Cytopenia - NOT Fanconi anaemia v0.16 SAMD9L Louise Daugherty Added phenotypes 159550 Ataxia-pancytopenia syndrome for gene: SAMD9L
Cytopenia - NOT Fanconi anaemia v0.16 SAMD9 Louise Daugherty Added phenotypes 617053 MIRAGE syndrome for gene: SAMD9
Cytopenia - NOT Fanconi anaemia v0.16 RTEL1 Louise Daugherty Added phenotypes 616373 Pulmonary fibrosis and/or bone marrow failure, telomere-related; 615190 DC type 4 and 5 for gene: RTEL1
Cytopenia - NOT Fanconi anaemia v0.16 RBM8A Louise Daugherty Added phenotypes 274000 Thrombocytopenia-absent radius syndrome for gene: RBM8A
Cytopenia - NOT Fanconi anaemia v0.16 PARN Louise Daugherty Added phenotypes 616371 Pulmonary fibrosis and/or bone marrow failure, telomere-related, 4; 616353 Dyskeratosis congenita, autosomal recessive 6 for gene: PARN
Cytopenia - NOT Fanconi anaemia v0.16 NBN Louise Daugherty Added phenotypes 251260 Nijmegen breakage syndrome for gene: NBN
Cytopenia - NOT Fanconi anaemia v0.16 MYSM1 Louise Daugherty Added phenotypes 618116 Bone marrow failure syndrome 4 for gene: MYSM1
Cytopenia - NOT Fanconi anaemia v0.16 MPL Louise Daugherty Added phenotypes 604498 Thrombocytopenia, congenital amegakaryocytic for gene: MPL
Cytopenia - NOT Fanconi anaemia v0.16 MECOM Louise Daugherty Added phenotypes 616738 Radioulnar synostosis with amegakaryocytic thrombocytopenia 2 for gene: MECOM
Cytopenia - NOT Fanconi anaemia v0.16 JAGN1 Louise Daugherty Added phenotypes 616022 Neutropenia, severe congenital, 6, autosomal recessive for gene: JAGN1
Cytopenia - NOT Fanconi anaemia v0.16 HOXA11 Louise Daugherty Added phenotypes 605432 Radioulnar synostosis with amegakaryocytic thrombocytopenia 1 for gene: HOXA11
Cytopenia - NOT Fanconi anaemia v0.16 HAX1 Louise Daugherty Added phenotypes 610738 Neutropenia, severe congenital 3, autosomal recessive for gene: HAX1
Cytopenia - NOT Fanconi anaemia v0.16 GFI1 Louise Daugherty Added phenotypes 607847 ?Neutropenia, nonimmune chronic idiopathic, of adults for gene: GFI1
Cytopenia - NOT Fanconi anaemia v0.16 GATA2 Louise Daugherty Added phenotypes 614038 Emberger syndrome for gene: GATA2
Cytopenia - NOT Fanconi anaemia v0.16 GATA1 Louise Daugherty Added phenotypes 314050 Thrombocytopenia with beta-thalassemia, X-linked for gene: GATA1
Cytopenia - NOT Fanconi anaemia v0.16 G6PC3 Louise Daugherty Added phenotypes 612541 Neutropenia, severe congenital 4, autosomal recessive for gene: G6PC3
Cytopenia - NOT Fanconi anaemia v0.16 FYB1 Louise Daugherty Added phenotypes 273900 Thrombocytopenia 3 for gene: FYB1
Cytopenia - NOT Fanconi anaemia v0.16 ETV6 Louise Daugherty Added phenotypes 616216 Thrombocytopenia 5 for gene: ETV6
Cytopenia - NOT Fanconi anaemia v0.16 ERCC6L2 Louise Daugherty Added phenotypes 615715 Bone marrow failure syndrome 2 for gene: ERCC6L2
Cytopenia - NOT Fanconi anaemia v0.16 ELANE Louise Daugherty Added phenotypes 202700 Neutropenia, severe congenital 1, autosomal dominant; 162800 Neutropenia, cyclic for gene: ELANE
Cytopenia - NOT Fanconi anaemia v0.16 EFL1 Louise Daugherty Added phenotypes 617941 Shwachman-Diamond syndrome 2 for gene: EFL1
Cytopenia - NOT Fanconi anaemia v0.16 DNAJC21 Louise Daugherty Added phenotypes 617052 Bone marrow failure syndrome 3 for gene: DNAJC21
Cytopenia - NOT Fanconi anaemia v0.16 DKC1 Louise Daugherty Added phenotypes 305000 Dyskeratosis congenita for gene: DKC1
Cytopenia - NOT Fanconi anaemia v0.16 CYCS Louise Daugherty Added phenotypes 612004 Thrombocytopenia 4 for gene: CYCS
Cytopenia - NOT Fanconi anaemia v0.16 CXCR4 Louise Daugherty Added phenotypes 193670 WHIM syndrome for gene: CXCR4
Cytopenia - NOT Fanconi anaemia v0.16 CTC1 Louise Daugherty Added phenotypes Dyskeratosis congenita for gene: CTC1
Cytopenia - NOT Fanconi anaemia v0.16 CSF3R Louise Daugherty Added phenotypes 617014 Neutropenia, severe congenital, 7, autosomal recessive for gene: CSF3R
Cytopenia - NOT Fanconi anaemia v0.16 ANKRD26 Louise Daugherty Added phenotypes 188000 Thrombocytopenia 2 for gene: ANKRD26
Cytopenia - NOT Fanconi anaemia v0.16 ACD Louise Daugherty Added phenotypes 616553 ?Dyskeratosis congenita 6 and 7 for gene: ACD
Cytopenia - NOT Fanconi anaemia v0.15 TP53 Louise Daugherty Source NHS GMS was added to TP53.
Cytopenia - NOT Fanconi anaemia v0.15 MYSM1 Louise Daugherty Source NHS GMS was added to MYSM1.
Cytopenia - NOT Fanconi anaemia v0.15 FYB1 Louise Daugherty Source NHS GMS was added to FYB1.
Cytopenia - NOT Fanconi anaemia v0.15 CYCS Louise Daugherty Source NHS GMS was added to CYCS.
Cytopenia - NOT Fanconi anaemia v0.14 WRAP53 Louise Daugherty Source Yorkshire and North East GLH was added to WRAP53.
Cytopenia - NOT Fanconi anaemia v0.14 WAS Louise Daugherty Source Yorkshire and North East GLH was added to WAS.
Cytopenia - NOT Fanconi anaemia v0.14 VPS45 Louise Daugherty Source Yorkshire and North East GLH was added to VPS45.
Cytopenia - NOT Fanconi anaemia v0.14 USB1 Louise Daugherty Source Yorkshire and North East GLH was added to USB1.
Cytopenia - NOT Fanconi anaemia v0.14 TP53 Louise Daugherty gene: TP53 was added
gene: TP53 was added to Cytopenia - NOT Fanconi anaemia. Sources: Yorkshire and North East GLH
Mode of inheritance for gene: TP53 was set to
Cytopenia - NOT Fanconi anaemia v0.14 TINF2 Louise Daugherty Source Yorkshire and North East GLH was added to TINF2.
Cytopenia - NOT Fanconi anaemia v0.14 THPO Louise Daugherty Source Yorkshire and North East GLH was added to THPO.
Cytopenia - NOT Fanconi anaemia v0.14 TERT Louise Daugherty Source Yorkshire and North East GLH was added to TERT.
Cytopenia - NOT Fanconi anaemia v0.14 TERC Louise Daugherty Source Yorkshire and North East GLH was added to TERC.
Cytopenia - NOT Fanconi anaemia v0.14 TAZ Louise Daugherty Source Yorkshire and North East GLH was added to TAZ.
Cytopenia - NOT Fanconi anaemia v0.14 SRP72 Louise Daugherty Source Yorkshire and North East GLH was added to SRP72.
Cytopenia - NOT Fanconi anaemia v0.14 SBDS Louise Daugherty Source Yorkshire and North East GLH was added to SBDS.
Cytopenia - NOT Fanconi anaemia v0.14 SAMD9L Louise Daugherty Source Yorkshire and North East GLH was added to SAMD9L.
Cytopenia - NOT Fanconi anaemia v0.14 SAMD9 Louise Daugherty Source Yorkshire and North East GLH was added to SAMD9.
Cytopenia - NOT Fanconi anaemia v0.14 RTEL1 Louise Daugherty Source Yorkshire and North East GLH was added to RTEL1.
Cytopenia - NOT Fanconi anaemia v0.14 RBM8A Louise Daugherty Source Yorkshire and North East GLH was added to RBM8A.
Cytopenia - NOT Fanconi anaemia v0.14 PARN Louise Daugherty Source Yorkshire and North East GLH was added to PARN.
Cytopenia - NOT Fanconi anaemia v0.14 NBN Louise Daugherty Source Yorkshire and North East GLH was added to NBN.
Cytopenia - NOT Fanconi anaemia v0.14 MYSM1 Louise Daugherty gene: MYSM1 was added
gene: MYSM1 was added to Cytopenia - NOT Fanconi anaemia. Sources: Yorkshire and North East GLH
Mode of inheritance for gene: MYSM1 was set to
Cytopenia - NOT Fanconi anaemia v0.14 MPL Louise Daugherty Source Yorkshire and North East GLH was added to MPL.
Cytopenia - NOT Fanconi anaemia v0.14 MECOM Louise Daugherty Source Yorkshire and North East GLH was added to MECOM.
Cytopenia - NOT Fanconi anaemia v0.14 JAGN1 Louise Daugherty Source Yorkshire and North East GLH was added to JAGN1.
Cytopenia - NOT Fanconi anaemia v0.14 HOXA11 Louise Daugherty Source Yorkshire and North East GLH was added to HOXA11.
Cytopenia - NOT Fanconi anaemia v0.14 HAX1 Louise Daugherty Source Yorkshire and North East GLH was added to HAX1.
Cytopenia - NOT Fanconi anaemia v0.14 GFI1 Louise Daugherty Source Yorkshire and North East GLH was added to GFI1.
Cytopenia - NOT Fanconi anaemia v0.14 GATA2 Louise Daugherty Source Yorkshire and North East GLH was added to GATA2.
Cytopenia - NOT Fanconi anaemia v0.14 GATA1 Louise Daugherty Source Yorkshire and North East GLH was added to GATA1.
Cytopenia - NOT Fanconi anaemia v0.14 G6PC3 Louise Daugherty Source Yorkshire and North East GLH was added to G6PC3.
Cytopenia - NOT Fanconi anaemia v0.14 FYB1 Louise Daugherty gene: FYB1 was added
gene: FYB1 was added to Cytopenia - NOT Fanconi anaemia. Sources: Yorkshire and North East GLH
Mode of inheritance for gene: FYB1 was set to
Cytopenia - NOT Fanconi anaemia v0.14 ETV6 Louise Daugherty Source Yorkshire and North East GLH was added to ETV6.
Cytopenia - NOT Fanconi anaemia v0.14 ERCC6L2 Louise Daugherty Source Yorkshire and North East GLH was added to ERCC6L2.
Cytopenia - NOT Fanconi anaemia v0.14 ELANE Louise Daugherty Source Yorkshire and North East GLH was added to ELANE.
Cytopenia - NOT Fanconi anaemia v0.14 EFL1 Louise Daugherty Source Yorkshire and North East GLH was added to EFL1.
Cytopenia - NOT Fanconi anaemia v0.14 DNAJC21 Louise Daugherty Source Yorkshire and North East GLH was added to DNAJC21.
Cytopenia - NOT Fanconi anaemia v0.14 DKC1 Louise Daugherty Source Yorkshire and North East GLH was added to DKC1.
Cytopenia - NOT Fanconi anaemia v0.14 CYCS Louise Daugherty gene: CYCS was added
gene: CYCS was added to Cytopenia - NOT Fanconi anaemia. Sources: Yorkshire and North East GLH
Mode of inheritance for gene: CYCS was set to
Cytopenia - NOT Fanconi anaemia v0.14 CXCR4 Louise Daugherty Source Yorkshire and North East GLH was added to CXCR4.
Cytopenia - NOT Fanconi anaemia v0.14 CTC1 Louise Daugherty Source Yorkshire and North East GLH was added to CTC1.
Cytopenia - NOT Fanconi anaemia v0.14 CSF3R Louise Daugherty Source Yorkshire and North East GLH was added to CSF3R.
Cytopenia - NOT Fanconi anaemia v0.14 ANKRD26 Louise Daugherty Source Yorkshire and North East GLH was added to ANKRD26.
Cytopenia - NOT Fanconi anaemia v0.14 ACD Louise Daugherty Source Yorkshire and North East GLH was added to ACD.
Cytopenia - NOT Fanconi anaemia v0.13 EFL1 Louise Daugherty Source Expert Review Green was added to EFL1.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.13 JAGN1 Louise Daugherty Source Expert Review Green was added to JAGN1.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.13 ETV6 Louise Daugherty Source Expert Review Green was added to ETV6.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.13 THPO Louise Daugherty Source Expert Review Green was added to THPO.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.13 STIM1 Louise Daugherty Source Expert Review Green was added to STIM1.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.13 DDX41 Louise Daugherty Source Expert Review Green was added to DDX41.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.13 MECOM Louise Daugherty Source Expert Review Green was added to MECOM.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.13 SLC37A4 Louise Daugherty Source Expert Review Green was added to SLC37A4.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.13 ACKR1 Louise Daugherty Source Expert Review Amber was added to ACKR1.
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.13 TUBB1 Louise Daugherty Source Expert Review Red was added to TUBB1.
Cytopenia - NOT Fanconi anaemia v0.13 RBM8A Louise Daugherty Source Expert Review Green was added to RBM8A.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.13 NBEAL2 Louise Daugherty Source Expert Review Green was added to NBEAL2.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.13 MYH9 Louise Daugherty Source Expert Review Green was added to MYH9.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.13 GP1BA Louise Daugherty Source Expert Review Green was added to GP1BA.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.13 ANKRD26 Louise Daugherty Source Expert Review Green was added to ANKRD26.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.13 RUNX1 Louise Daugherty Source Expert Review Green was added to RUNX1.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.13 SMARCAL1 Louise Daugherty Source Expert Review Green was added to SMARCAL1.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.13 PARN Louise Daugherty Source Expert Review Green was added to PARN.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.13 MPL Louise Daugherty Source Expert Review Green was added to MPL.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.13 LIG4 Louise Daugherty Source Expert Review Green was added to LIG4.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.13 HOXA11 Louise Daugherty Source Expert Review Red was added to HOXA11.
Cytopenia - NOT Fanconi anaemia v0.13 ACD Louise Daugherty Source Expert Review Green was added to ACD.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.12 EFL1 Louise Daugherty Mode of inheritance for gene EFL1 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes 617941 Shwachman-Diamond syndrome 2 for gene: EFL1
Cytopenia - NOT Fanconi anaemia v0.12 JAGN1 Louise Daugherty Mode of inheritance for gene JAGN1 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes 616022 Neutropenia, severe congenital, 6 for gene: JAGN1
Cytopenia - NOT Fanconi anaemia v0.12 ETV6 Louise Daugherty Mode of inheritance for gene ETV6 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Added phenotypes 616216 Thrombocytopenia 5 for gene: ETV6
Cytopenia - NOT Fanconi anaemia v0.12 THPO Louise Daugherty Mode of inheritance for gene THPO was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Added phenotypes 187950 Thrombocythemia 1 for gene: THPO
Cytopenia - NOT Fanconi anaemia v0.12 STIM1 Louise Daugherty Mode of inheritance for gene STIM1 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Added phenotypes 185070 Stormorken syndrome for gene: STIM1
Cytopenia - NOT Fanconi anaemia v0.12 DDX41 Louise Daugherty Mode of inheritance for gene DDX41 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Added phenotypes 616871 Susceptibility to myeloid neoplasms for gene: DDX41
Cytopenia - NOT Fanconi anaemia v0.12 MECOM Louise Daugherty Mode of inheritance for gene MECOM was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Added phenotypes 616738 Radioulnar synostosis with amegakaryocytic thrombocytopenia 2 for gene: MECOM
Cytopenia - NOT Fanconi anaemia v0.12 SLC37A4 Louise Daugherty Mode of inheritance for gene SLC37A4 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes 232220 Glycogen storage disease Ib for gene: SLC37A4
Cytopenia - NOT Fanconi anaemia v0.12 ACKR1 Louise Daugherty Mode of inheritance for gene ACKR1 was changed from to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Added phenotypes 613665 Benign hereditary neutropenia for gene: ACKR1
Cytopenia - NOT Fanconi anaemia v0.12 TUBB1 Louise Daugherty Mode of inheritance for gene TUBB1 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Added phenotypes 613112 Macrothrombocytopenia for gene: TUBB1
Cytopenia - NOT Fanconi anaemia v0.12 RBM8A Louise Daugherty Mode of inheritance for gene RBM8A was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes 274000 Thrombocytopenia-absent radius syndrome for gene: RBM8A
Cytopenia - NOT Fanconi anaemia v0.12 NBEAL2 Louise Daugherty Mode of inheritance for gene NBEAL2 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes 139090 Gray platelet syndrome for gene: NBEAL2
Cytopenia - NOT Fanconi anaemia v0.12 MYH9 Louise Daugherty Mode of inheritance for gene MYH9 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Added phenotypes 155100 Macrothrombocytopenia for gene: MYH9
Cytopenia - NOT Fanconi anaemia v0.12 GP1BA Louise Daugherty Mode of inheritance for gene GP1BA was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes 231200 Bernard-Soulier syndrome, type A1 for gene: GP1BA
Cytopenia - NOT Fanconi anaemia v0.12 ANKRD26 Louise Daugherty Mode of inheritance for gene ANKRD26 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Added phenotypes 188000 Thrombocytopenia 2 for gene: ANKRD26
Cytopenia - NOT Fanconi anaemia v0.12 RUNX1 Louise Daugherty Mode of inheritance for gene RUNX1 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Added phenotypes 601399 Platelet disorder, familial, with associated myeloid malignancy for gene: RUNX1
Cytopenia - NOT Fanconi anaemia v0.12 SMARCAL1 Louise Daugherty Mode of inheritance for gene SMARCAL1 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes 242900 Schimke immunoosseous dysplasia for gene: SMARCAL1
Cytopenia - NOT Fanconi anaemia v0.12 PARN Louise Daugherty Mode of inheritance for gene PARN was changed from to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Added phenotypes 616371 Pulmonary fibrosis and/or bone marrow failure, telomere-related, 4; 616353 Dyskeratosis congenita, autosomal recessive 6, for gene: PARN
Cytopenia - NOT Fanconi anaemia v0.12 MPL Louise Daugherty Mode of inheritance for gene MPL was changed from to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Added phenotypes 601977 Thrombocythemia 2; 604498 Thrombocytopenia, congenital amegakaryocytic for gene: MPL
Cytopenia - NOT Fanconi anaemia v0.12 LIG4 Louise Daugherty Mode of inheritance for gene LIG4 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes 606593 LIG4 syndrome for gene: LIG4
Cytopenia - NOT Fanconi anaemia v0.12 HOXA11 Louise Daugherty Mode of inheritance for gene HOXA11 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Added phenotypes 605432 Radioulnar synostosis with amegakaryocytic thrombocytopenia 1 for gene: HOXA11
Cytopenia - NOT Fanconi anaemia v0.12 ACD Louise Daugherty Mode of inheritance for gene ACD was changed from to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Added phenotypes 616553 ?Dyskeratosis congenita 6 and 7 for gene: ACD
Cytopenia - NOT Fanconi anaemia v0.11 USB1 Louise Daugherty commented on gene: USB1: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: USB1; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 604173 Poikiloderma with neutropenia; PMID(s): 20004881; 20503306
Cytopenia - NOT Fanconi anaemia v0.11 EFL1 Louise Daugherty reviewed gene: EFL1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.11 JAGN1 Louise Daugherty reviewed gene: JAGN1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.11 VPS45 Louise Daugherty commented on gene: VPS45: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: VPS45; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 615285 Neutropenia, severe congenital, 5; PMID(s): 23738510; 23599270
Cytopenia - NOT Fanconi anaemia v0.11 CSF3R Louise Daugherty commented on gene: CSF3R: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: CSF3R; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 617014 Neutropenia, severe congenital, 7; PMID(s): 19620628; 12203110; 26324699
Cytopenia - NOT Fanconi anaemia v0.11 ETV6 Louise Daugherty reviewed gene: ETV6: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.11 MPIG6B Louise Daugherty commented on gene: MPIG6B: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: MPIG6B; Suggested intial gene rating: Red List (low evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 617441 Thrombocytopenia, anemia, and myelofibrosis; PMID(s): 27743390
Cytopenia - NOT Fanconi anaemia v0.11 THPO Louise Daugherty reviewed gene: THPO: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.11 SAMD9L Louise Daugherty commented on gene: SAMD9L: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: SAMD9L; Suggested intial gene rating: Red List (low evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Phenotypes: 159550 Ataxia-pancytopenia syndrome; PMID(s): 27259050
Cytopenia - NOT Fanconi anaemia v0.11 STIM1 Louise Daugherty reviewed gene: STIM1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.11 DNAJC21 Louise Daugherty commented on gene: DNAJC21: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: DNAJC21; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 617052 Bone marrow failure syndrome 3; PMID(s): 27346687
Cytopenia - NOT Fanconi anaemia v0.11 DDX41 Louise Daugherty reviewed gene: DDX41: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.11 ERCC6L2 Louise Daugherty commented on gene: ERCC6L2: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: ERCC6L2; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 615715 Bone marrow failure syndrome 2; PMID(s): 24507776; 27185855
Cytopenia - NOT Fanconi anaemia v0.11 MECOM Louise Daugherty reviewed gene: MECOM: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.11 SAMD9 Louise Daugherty commented on gene: SAMD9: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: SAMD9; Suggested intial gene rating: Red List (low evidence); Are variants in this gene part of your current diagnostic practice? No; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Phenotypes: 617053 MIRAGE syndrome; PMID(s): 27182967
Cytopenia - NOT Fanconi anaemia v0.11 TAZ Louise Daugherty commented on gene: TAZ: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: TAZ; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females; Phenotypes: 302060 Barth syndrome; PMID(s): 9382096; 9345098
Cytopenia - NOT Fanconi anaemia v0.11 SLC37A4 Louise Daugherty reviewed gene: SLC37A4: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.11 HAX1 Louise Daugherty commented on gene: HAX1: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: HAX1; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 610738 Neutropenia, severe congenital 3; PMID(s): 17187068; 18337561; 18611981
Cytopenia - NOT Fanconi anaemia v0.11 GFI1 Louise Daugherty commented on gene: GFI1: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: GFI1; Suggested intial gene rating: Red List (low evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Phenotypes: 613107 Neutropenia, severe congenital 2; PMID(s): 12778173
Cytopenia - NOT Fanconi anaemia v0.11 G6PC3 Louise Daugherty commented on gene: G6PC3: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: G6PC3; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 612541 Neutropenia, severe congenital 4; PMID(s): 19696212; 20717171; 19118303
Cytopenia - NOT Fanconi anaemia v0.11 ELANE Louise Daugherty commented on gene: ELANE: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: ELANE; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Phenotypes: 162800 Cyclic neutropenia;202700 Neutropenia, severe congenital 1; PMID(s): 10581030; 11001877; 18028488
Cytopenia - NOT Fanconi anaemia v0.11 CXCR4 Louise Daugherty commented on gene: CXCR4: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: CXCR4; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Phenotypes: 193670 WHIM syndrome; PMID(s): 10767001; 12692554
Cytopenia - NOT Fanconi anaemia v0.11 ADA2 Louise Daugherty commented on gene: ADA2: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: ADA2; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 615688 Polyarteritis nodosa/Sneddon sydrome; PMID(s): 24552284; 24552285; 25075847
Cytopenia - NOT Fanconi anaemia v0.11 ACKR1 Louise Daugherty reviewed gene: ACKR1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.11 WAS Louise Daugherty commented on gene: WAS: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: WAS; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females; Phenotypes: 313900 Thrombocytopenia; PMID(s): 8757563; 8528199; 11167787
Cytopenia - NOT Fanconi anaemia v0.11 TUBB1 Louise Daugherty reviewed gene: TUBB1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.11 RBM8A Louise Daugherty reviewed gene: RBM8A: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.11 NBEAL2 Louise Daugherty reviewed gene: NBEAL2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.11 MYH9 Louise Daugherty reviewed gene: MYH9: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.11 GP1BA Louise Daugherty reviewed gene: GP1BA: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.11 ANKRD26 Louise Daugherty reviewed gene: ANKRD26: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.11 RUNX1 Louise Daugherty reviewed gene: RUNX1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.11 GATA2 Louise Daugherty commented on gene: GATA2: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: GATA2; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Phenotypes: 614038 Emberger syndrome; PMID(s): 21892158; 21892162
Cytopenia - NOT Fanconi anaemia v0.11 WRAP53 Louise Daugherty commented on gene: WRAP53: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: WRAP53; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 613988 Dyskeratosis congenita, autosomal recessive 3; PMID(s): 29514627; 21205863
Cytopenia - NOT Fanconi anaemia v0.11 TINF2 Louise Daugherty commented on gene: TINF2: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: TINF2; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Phenotypes: 613990 Dyskeratosis congenita, autosomal dominant 3; 268130 Revesz syndrome; PMID(s): 21536674; 18669893
Cytopenia - NOT Fanconi anaemia v0.11 TERT Louise Daugherty commented on gene: TERT: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: TERT; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Phenotypes: 613989 Dyskeratosis congenita;614742 Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1; PMID(s): 21436073; 18042801; 18460650
Cytopenia - NOT Fanconi anaemia v0.11 TERC Louise Daugherty commented on gene: TERC: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: TERC; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Phenotypes: 127550 Dyskeratosis congenita, autosomal dominant 1; PMID(s): 11574891; 12090986
Cytopenia - NOT Fanconi anaemia v0.11 SRP72 Louise Daugherty commented on gene: SRP72: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: SRP72; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Phenotypes: 614675 Bone marrow failure syndrome 1; PMID(s): 22541560
Cytopenia - NOT Fanconi anaemia v0.11 SMARCAL1 Louise Daugherty reviewed gene: SMARCAL1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.11 SBDS Louise Daugherty commented on gene: SBDS: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: SBDS; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 260400 Shwachman-Diamond syndrome; PMID(s): 12496757
Cytopenia - NOT Fanconi anaemia v0.11 RTEL1 Louise Daugherty commented on gene: RTEL1: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: RTEL1; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Phenotypes: 615190 Dyskeratosis congenita;616373 Pulmonary fibrosis and/or bone marrow failure, telomere-related, 3; PMID(s): 23329068; 23959892; 23453664
Cytopenia - NOT Fanconi anaemia v0.11 RMRP Louise Daugherty commented on gene: RMRP: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: RMRP; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 250250 Cartilage-hair hypoplasia; PMID(s): 11207361; 16832578
Cytopenia - NOT Fanconi anaemia v0.11 PARN Louise Daugherty reviewed gene: PARN: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.11 NOP10 Louise Daugherty commented on gene: NOP10: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: NOP10; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 224230 Dyskeratosis congenita, autosomal recessive 1; PMID(s): 17507419
Cytopenia - NOT Fanconi anaemia v0.11 NHP2 Louise Daugherty commented on gene: NHP2: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: NHP2; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 613987 Dyskeratosis congenita, autosomal recessive 2; PMID(s): 18523010
Cytopenia - NOT Fanconi anaemia v0.11 MPL Louise Daugherty reviewed gene: MPL: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.11 MASTL Louise Daugherty commented on gene: MASTL: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: MASTL; Suggested intial gene rating: Red List (low evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: Unknown; Phenotypes: Thrombocytopenia; PMID(s): 10891439; 22102272; 26136524
Cytopenia - NOT Fanconi anaemia v0.11 LIG4 Louise Daugherty reviewed gene: LIG4: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.11 HOXA11 Louise Daugherty reviewed gene: HOXA11: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.11 DKC1 Louise Daugherty commented on gene: DKC1: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: DKC1; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females; Phenotypes: 305000 Dyskeratosis congenita; PMID(s): 9888995; 11379875; 10364516
Cytopenia - NOT Fanconi anaemia v0.11 CTC1 Louise Daugherty commented on gene: CTC1: Initial gene list (Consensus Genes for Haem Panels 17.12.18_KCH.xlsx) collated by Frances Smith Viapath Kings College Hospital February 2019 on behalf of London South GLH for the GMS Haematology specialist test group. Gene Symbol submitted: CTC1; Suggested intial gene rating: Green List (high evidence); Are variants in this gene part of your current diagnostic practice? Yes; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Phenotypes: 612199 Coats plus syndrome; PMID(s): 22532422; 22267198; 22387016; 22899577
Cytopenia - NOT Fanconi anaemia v0.11 ACD Louise Daugherty reviewed gene: ACD: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.10 USB1 Frances Smith reviewed gene: USB1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 604173 Poikiloderma with neutropenia; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 EFL1 Frances Smith reviewed gene: EFL1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 617941 Shwachman-Diamond syndrome 2; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.10 JAGN1 Frances Smith reviewed gene: JAGN1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 616022 Neutropenia, severe congenital, 6; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.10 VPS45 Frances Smith reviewed gene: VPS45: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 615285 Neutropenia, severe congenital, 5; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.10 CSF3R Frances Smith reviewed gene: CSF3R: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 617014 Neutropenia, severe congenital, 7; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.10 ETV6 Frances Smith reviewed gene: ETV6: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 616216 Thrombocytopenia 5; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v0.10 MPIG6B Frances Smith reviewed gene: MPIG6B: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: 617441 Thrombocytopenia, anemia, and myelofibrosis; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.10 THPO Frances Smith reviewed gene: THPO: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 187950 Thrombocythemia 1; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v0.10 SAMD9L Frances Smith reviewed gene: SAMD9L: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: 159550 Ataxia-pancytopenia syndrome; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v0.10 STIM1 Frances Smith reviewed gene: STIM1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 185070 Stormorken syndrome; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v0.10 DNAJC21 Frances Smith reviewed gene: DNAJC21: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 617052 Bone marrow failure syndrome 3; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.10 DDX41 Frances Smith reviewed gene: DDX41: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 616871 Susceptibility to myeloid neoplasms; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v0.10 ERCC6L2 Frances Smith reviewed gene: ERCC6L2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 615715 Bone marrow failure syndrome 2; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cytopenia - NOT Fanconi anaemia v0.10 MECOM Frances Smith reviewed gene: MECOM: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 616738 Radioulnar synostosis with amegakaryocytic thrombocytopenia 2; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v0.10 SAMD9 Frances Smith reviewed gene: SAMD9: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: 617053 MIRAGE syndrome; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cytopenia - NOT Fanconi anaemia v0.10 TAZ Frances Smith reviewed gene: TAZ: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 302060 Barth syndrome; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 SLC37A4 Frances Smith reviewed gene: SLC37A4: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 232220 Glycogen storage disease Ib; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 HAX1 Frances Smith reviewed gene: HAX1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 610738 Neutropenia, severe congenital 3; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 GFI1 Frances Smith reviewed gene: GFI1: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: 613107 Neutropenia, severe congenital 2; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 G6PC3 Frances Smith reviewed gene: G6PC3: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 612541 Neutropenia, severe congenital 4; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 ELANE Frances Smith reviewed gene: ELANE: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 162800 Cyclic neutropenia, 202700 Neutropenia, severe congenital 1; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 CXCR4 Frances Smith reviewed gene: CXCR4: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 193670 WHIM syndrome; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 ADA2 Frances Smith reviewed gene: ADA2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 615688 Polyarteritis nodosa/Sneddon sydrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 ACKR1 Frances Smith reviewed gene: ACKR1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: 613665 Benign hereditary neutropenia; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 WAS Frances Smith reviewed gene: WAS: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 313900 Thrombocytopenia; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 TUBB1 Frances Smith reviewed gene: TUBB1: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: 613112 Macrothrombocytopenia; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 RBM8A Frances Smith reviewed gene: RBM8A: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 274000 Thrombocytopenia-absent radius syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 NBEAL2 Frances Smith reviewed gene: NBEAL2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 139090 Gray platelet syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 MYH9 Frances Smith reviewed gene: MYH9: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 155100 Macrothrombocytopenia; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 GP1BA Frances Smith reviewed gene: GP1BA: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 231200 Bernard-Soulier syndrome, type A1; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 ANKRD26 Frances Smith reviewed gene: ANKRD26: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 188000 Thrombocytopenia 2; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 RUNX1 Frances Smith reviewed gene: RUNX1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 601399 Platelet disorder, familial, with associated myeloid malignancy; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 GATA2 Frances Smith reviewed gene: GATA2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 614038 Emberger syndrome; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 WRAP53 Frances Smith reviewed gene: WRAP53: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 613988 Dyskeratosis congenita, autosomal recessive 3; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 TINF2 Frances Smith reviewed gene: TINF2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 613990 Dyskeratosis congenita, autosomal dominant 3, 268130 Revesz syndrome; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 TERT Frances Smith reviewed gene: TERT: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 613989 Dyskeratosis congenita, 614742 Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 TERC Frances Smith reviewed gene: TERC: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 127550 Dyskeratosis congenita, autosomal dominant 1; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 SRP72 Frances Smith reviewed gene: SRP72: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 614675 Bone marrow failure syndrome 1; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 SMARCAL1 Frances Smith reviewed gene: SMARCAL1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 242900 Schimke immunoosseous dysplasia; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 SBDS Frances Smith reviewed gene: SBDS: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 260400 Shwachman-Diamond syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 RTEL1 Frances Smith reviewed gene: RTEL1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 615190 Dyskeratosis congenita, 616373 Pulmonary fibrosis and/or bone marrow failure, telomere-related, 3; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 RMRP Frances Smith reviewed gene: RMRP: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 250250 Cartilage-hair hypoplasia; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 PARN Frances Smith reviewed gene: PARN: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 616353 Dyskeratosis congenita, autosomal recessive 6,, 616371 Pulmonary fibrosis and/or bone marrow failure, telomere-related, 4; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 NOP10 Frances Smith reviewed gene: NOP10: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 224230 Dyskeratosis congenita, autosomal recessive 1; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 NHP2 Frances Smith reviewed gene: NHP2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 613987 Dyskeratosis congenita, autosomal recessive 2; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 MPL Frances Smith reviewed gene: MPL: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 601977 Thrombocythemia 2, 604498 Thrombocytopenia, congenital amegakaryocytic; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 MASTL Frances Smith reviewed gene: MASTL: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Thrombocytopenia; Mode of inheritance: Unknown; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 LIG4 Frances Smith reviewed gene: LIG4: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 606593 LIG4 syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 HOXA11 Frances Smith reviewed gene: HOXA11: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: 605432 Radioulnar synostosis with amegakaryocytic thrombocytopenia 1; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 DKC1 Frances Smith reviewed gene: DKC1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 305000 Dyskeratosis congenita; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 CTC1 Frances Smith reviewed gene: CTC1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 612199 Coats plus syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.10 ACD Frances Smith reviewed gene: ACD: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: 616553 ?Dyskeratosis congenita 6 and 7; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.9 USB1 Louise Daugherty Added phenotypes 604173 Poikiloderma with neutropenia for gene: USB1
Publications for gene USB1 were changed from to 20503306; 20004881
Cytopenia - NOT Fanconi anaemia v0.9 EFL1 Louise Daugherty Added phenotypes 617941 Shwachman-Diamond syndrome 2 for gene: EFL1
Publications for gene EFL1 were changed from to 28331068
Cytopenia - NOT Fanconi anaemia v0.9 JAGN1 Louise Daugherty Added phenotypes 616022 Neutropenia, severe congenital, 6 for gene: JAGN1
Publications for gene JAGN1 were changed from to 25129144
Cytopenia - NOT Fanconi anaemia v0.9 VPS45 Louise Daugherty Added phenotypes 615285 Neutropenia, severe congenital, 5 for gene: VPS45
Cytopenia - NOT Fanconi anaemia v0.9 CSF3R Louise Daugherty Added phenotypes 617014 Neutropenia, severe congenital, 7 for gene: CSF3R
Publications for gene CSF3R were changed from 26324699; 24753537; 9001427 to 26324699; 12203110; 19620628
Cytopenia - NOT Fanconi anaemia v0.9 ETV6 Louise Daugherty Added phenotypes 616216 Thrombocytopenia 5 for gene: ETV6
Publications for gene ETV6 were changed from to 25581430; 25807284
Cytopenia - NOT Fanconi anaemia v0.9 MPIG6B Louise Daugherty Added phenotypes 617441 Thrombocytopenia, anemia, and myelofibrosis for gene: MPIG6B
Cytopenia - NOT Fanconi anaemia v0.9 THPO Louise Daugherty Added phenotypes 187950 Thrombocythemia 1 for gene: THPO
Publications for gene THPO were changed from to 19553636; 10583217
Cytopenia - NOT Fanconi anaemia v0.9 SAMD9L Louise Daugherty Added phenotypes 159550 Ataxia-pancytopenia syndrome for gene: SAMD9L
Publications for gene SAMD9L were changed from 27259050; 28202457 to 27259050
Cytopenia - NOT Fanconi anaemia v0.9 STIM1 Louise Daugherty Added phenotypes 185070 Stormorken syndrome for gene: STIM1
Publications for gene STIM1 were changed from to 25577287
Cytopenia - NOT Fanconi anaemia v0.9 DNAJC21 Louise Daugherty Added phenotypes 617052 Bone marrow failure syndrome 3 for gene: DNAJC21
Publications for gene DNAJC21 were changed from 27346687; 29700810; 28062395 to 27346687
Cytopenia - NOT Fanconi anaemia v0.9 DDX41 Louise Daugherty Added phenotypes 616871 Susceptibility to myeloid neoplasms for gene: DDX41
Publications for gene DDX41 were changed from to 25920683; 26712909
Cytopenia - NOT Fanconi anaemia v0.9 ERCC6L2 Louise Daugherty Added phenotypes 615715 Bone marrow failure syndrome 2 for gene: ERCC6L2
Cytopenia - NOT Fanconi anaemia v0.9 MECOM Louise Daugherty Added phenotypes 616738 Radioulnar synostosis with amegakaryocytic thrombocytopenia 2 for gene: MECOM
Publications for gene MECOM were changed from to 20091385; 26581901
Cytopenia - NOT Fanconi anaemia v0.9 SAMD9 Louise Daugherty Added phenotypes 617053 MIRAGE syndrome for gene: SAMD9
Cytopenia - NOT Fanconi anaemia v0.9 TAZ Louise Daugherty Added phenotypes 302060 Barth syndrome for gene: TAZ
Publications for gene TAZ were changed from to 9345098; 9382096
Cytopenia - NOT Fanconi anaemia v0.9 SLC37A4 Louise Daugherty Added phenotypes 232220 Glycogen storage disease Ib for gene: SLC37A4
Publications for gene SLC37A4 were changed from to 9428641; 9675154
Cytopenia - NOT Fanconi anaemia v0.9 HAX1 Louise Daugherty Added phenotypes 610738 Neutropenia, severe congenital 3 for gene: HAX1
Publications for gene HAX1 were changed from 17187068; 10581030; 18024606; 18337561 to 18611981; 17187068; 18337561
Cytopenia - NOT Fanconi anaemia v0.9 GFI1 Louise Daugherty Added phenotypes 613107 Neutropenia, severe congenital 2 for gene: GFI1
Publications for gene GFI1 were changed from 12530980; 12778173; 11810106; 19775295 to 12778173
Cytopenia - NOT Fanconi anaemia v0.9 G6PC3 Louise Daugherty Added phenotypes 612541 Neutropenia, severe congenital 4 for gene: G6PC3
Publications for gene G6PC3 were changed from 19118303 to 19696212; 19118303; 20717171
Cytopenia - NOT Fanconi anaemia v0.9 ELANE Louise Daugherty Added phenotypes 202700 Neutropenia, severe congenital 1; 162800 Cyclic neutropenia for gene: ELANE
Publications for gene ELANE were changed from 10581030; 11675333 to 18028488; 11001877; 10581030
Cytopenia - NOT Fanconi anaemia v0.9 CXCR4 Louise Daugherty Added phenotypes 193670 WHIM syndrome for gene: CXCR4
Publications for gene CXCR4 were changed from 12692554; 15536153 to 10767001; 12692554
Cytopenia - NOT Fanconi anaemia v0.9 ADA2 Louise Daugherty Added phenotypes 615688 Polyarteritis nodosa/Sneddon sydrome for gene: ADA2
Publications for gene ADA2 were changed from to 25075847; 24552285; 24552284
Cytopenia - NOT Fanconi anaemia v0.9 ACKR1 Louise Daugherty Added phenotypes 613665 Benign hereditary neutropenia for gene: ACKR1
Cytopenia - NOT Fanconi anaemia v0.9 WAS Louise Daugherty Added phenotypes 313900 Thrombocytopenia for gene: WAS
Publications for gene WAS were changed from 16804117 to 8528199; 8757563; 11167787
Cytopenia - NOT Fanconi anaemia v0.9 TUBB1 Louise Daugherty Added phenotypes 613112 Macrothrombocytopenia for gene: TUBB1
Publications for gene TUBB1 were changed from to 18849486
Cytopenia - NOT Fanconi anaemia v0.9 RBM8A Louise Daugherty Added phenotypes 274000 Thrombocytopenia-absent radius syndrome for gene: RBM8A
Publications for gene RBM8A were changed from to 22366785; 17236129
Cytopenia - NOT Fanconi anaemia v0.9 NBEAL2 Louise Daugherty Added phenotypes 139090 Gray platelet syndrome for gene: NBEAL2
Publications for gene NBEAL2 were changed from to 20709904
Cytopenia - NOT Fanconi anaemia v0.9 MYH9 Louise Daugherty Added phenotypes 155100 Macrothrombocytopenia for gene: MYH9
Publications for gene MYH9 were changed from to 20174760
Cytopenia - NOT Fanconi anaemia v0.9 GP1BA Louise Daugherty Added phenotypes 231200 Bernard-Soulier syndrome, type A1 for gene: GP1BA
Publications for gene GP1BA were changed from to 2308962
Cytopenia - NOT Fanconi anaemia v0.9 ANKRD26 Louise Daugherty Added phenotypes 188000 Thrombocytopenia 2 for gene: ANKRD26
Publications for gene ANKRD26 were changed from to 2121161; 20626622
Cytopenia - NOT Fanconi anaemia v0.9 RUNX1 Louise Daugherty Added phenotypes 601399 Platelet disorder, familial, with associated myeloid malignancy for gene: RUNX1
Publications for gene RUNX1 were changed from to 19357396; 9746808
Cytopenia - NOT Fanconi anaemia v0.9 GATA2 Louise Daugherty Added phenotypes 614038 Emberger syndrome for gene: GATA2
Publications for gene GATA2 were changed from 27418648; 21892162 to 21892158; 21892162
Cytopenia - NOT Fanconi anaemia v0.9 WRAP53 Louise Daugherty Added phenotypes 613988 Dyskeratosis congenita, autosomal recessive 3 for gene: WRAP53
Publications for gene WRAP53 were changed from to 29514627; 21205863
Cytopenia - NOT Fanconi anaemia v0.9 TINF2 Louise Daugherty Added phenotypes 613990 Dyskeratosis congenita, autosomal dominant 3; 268130 Revesz syndrome for gene: TINF2
Publications for gene TINF2 were changed from to 18669893; 21536674
Cytopenia - NOT Fanconi anaemia v0.9 TERT Louise Daugherty Added phenotypes 614742 Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1; 613989 Dyskeratosis congenita for gene: TERT
Publications for gene TERT were changed from 15885610; 19179534; 15814878 to 21436073; 18460650; 18042801
Cytopenia - NOT Fanconi anaemia v0.9 TERC Louise Daugherty Added phenotypes 127550 Dyskeratosis congenita, autosomal dominant 1 for gene: TERC
Publications for gene TERC were changed from to 11574891; 12090986
Cytopenia - NOT Fanconi anaemia v0.9 SRP72 Louise Daugherty Added phenotypes 614675 Bone marrow failure syndrome 1 for gene: SRP72
Publications for gene SRP72 were changed from to 22541560
Cytopenia - NOT Fanconi anaemia v0.9 SMARCAL1 Louise Daugherty Added phenotypes 242900 Schimke immunoosseous dysplasia for gene: SMARCAL1
Publications for gene SMARCAL1 were changed from to 17089404
Cytopenia - NOT Fanconi anaemia v0.9 SBDS Louise Daugherty Added phenotypes 260400 Shwachman-Diamond syndrome for gene: SBDS
Publications for gene SBDS were changed from 14749921; 12496757 to 12496757
Cytopenia - NOT Fanconi anaemia v0.9 RTEL1 Louise Daugherty Added phenotypes 616373 Pulmonary fibrosis and/or bone marrow failure, telomere-related, 3; 615190 Dyskeratosis congenita for gene: RTEL1
Publications for gene RTEL1 were changed from 23591994; 23453664; 23329068 to 23453664; 23329068; 23959892
Cytopenia - NOT Fanconi anaemia v0.9 RMRP Louise Daugherty Added phenotypes 250250 Cartilage-hair hypoplasia for gene: RMRP
Publications for gene RMRP were changed from 11207361 to 11207361; 16832578
Cytopenia - NOT Fanconi anaemia v0.9 PARN Louise Daugherty Added phenotypes 616371 Pulmonary fibrosis and/or bone marrow failure, telomere-related, 4; 616353 Dyskeratosis congenita, autosomal recessive 6, for gene: PARN
Publications for gene PARN were changed from to 25848748; 26342108; 25893599
Cytopenia - NOT Fanconi anaemia v0.9 NOP10 Louise Daugherty Added phenotypes 224230 Dyskeratosis congenita, autosomal recessive 1 for gene: NOP10
Cytopenia - NOT Fanconi anaemia v0.9 NHP2 Louise Daugherty Added phenotypes 613987 Dyskeratosis congenita, autosomal recessive 2 for gene: NHP2
Cytopenia - NOT Fanconi anaemia v0.9 MPL Louise Daugherty Added phenotypes 601977 Thrombocythemia 2; 604498 Thrombocytopenia, congenital amegakaryocytic for gene: MPL
Publications for gene MPL were changed from to 11133753; 10077649
Cytopenia - NOT Fanconi anaemia v0.9 MASTL Louise Daugherty Added phenotypes Thrombocytopenia for gene: MASTL
Publications for gene MASTL were changed from 12890928; 26136524; 21211618 to 10891439; 26136524; 22102272
Cytopenia - NOT Fanconi anaemia v0.9 LIG4 Louise Daugherty Added phenotypes 606593 LIG4 syndrome for gene: LIG4
Publications for gene LIG4 were changed from to 20133615; 16088910; 11779494
Cytopenia - NOT Fanconi anaemia v0.9 HOXA11 Louise Daugherty Added phenotypes 605432 Radioulnar synostosis with amegakaryocytic thrombocytopenia 1 for gene: HOXA11
Publications for gene HOXA11 were changed from to 20091385; 11101832
Cytopenia - NOT Fanconi anaemia v0.9 DKC1 Louise Daugherty Added phenotypes 305000 Dyskeratosis congenita for gene: DKC1
Publications for gene DKC1 were changed from 10583221; 9590285; 9590276; 10217077 to 10364516; 9888995; 11379875
Cytopenia - NOT Fanconi anaemia v0.9 CTC1 Louise Daugherty Added phenotypes 612199 Coats plus syndrome for gene: CTC1
Publications for gene CTC1 were changed from 22532422; 22899577 to 22532422; 22899577; 22267198; 22387016
Cytopenia - NOT Fanconi anaemia v0.9 ACD Louise Daugherty Added phenotypes 616553 ?Dyskeratosis congenita 6 and 7 for gene: ACD
Publications for gene ACD were changed from to 25233904; 25205116
Cytopenia - NOT Fanconi anaemia v0.8 EFL1 Louise Daugherty Source NHS GMS was added to EFL1.
Cytopenia - NOT Fanconi anaemia v0.8 JAGN1 Louise Daugherty Source NHS GMS was added to JAGN1.
Cytopenia - NOT Fanconi anaemia v0.8 ETV6 Louise Daugherty Source NHS GMS was added to ETV6.
Cytopenia - NOT Fanconi anaemia v0.8 THPO Louise Daugherty Source NHS GMS was added to THPO.
Cytopenia - NOT Fanconi anaemia v0.8 STIM1 Louise Daugherty Source NHS GMS was added to STIM1.
Cytopenia - NOT Fanconi anaemia v0.8 DDX41 Louise Daugherty Source NHS GMS was added to DDX41.
Cytopenia - NOT Fanconi anaemia v0.8 MECOM Louise Daugherty Source NHS GMS was added to MECOM.
Cytopenia - NOT Fanconi anaemia v0.8 SLC37A4 Louise Daugherty Source NHS GMS was added to SLC37A4.
Cytopenia - NOT Fanconi anaemia v0.8 ACKR1 Louise Daugherty Source NHS GMS was added to ACKR1.
Cytopenia - NOT Fanconi anaemia v0.8 TUBB1 Louise Daugherty Source NHS GMS was added to TUBB1.
Cytopenia - NOT Fanconi anaemia v0.8 RBM8A Louise Daugherty Source NHS GMS was added to RBM8A.
Cytopenia - NOT Fanconi anaemia v0.8 NBEAL2 Louise Daugherty Source NHS GMS was added to NBEAL2.
Cytopenia - NOT Fanconi anaemia v0.8 MYH9 Louise Daugherty Source NHS GMS was added to MYH9.
Cytopenia - NOT Fanconi anaemia v0.8 GP1BA Louise Daugherty Source NHS GMS was added to GP1BA.
Cytopenia - NOT Fanconi anaemia v0.8 ANKRD26 Louise Daugherty Source NHS GMS was added to ANKRD26.
Cytopenia - NOT Fanconi anaemia v0.8 RUNX1 Louise Daugherty Source NHS GMS was added to RUNX1.
Cytopenia - NOT Fanconi anaemia v0.8 SMARCAL1 Louise Daugherty Source NHS GMS was added to SMARCAL1.
Cytopenia - NOT Fanconi anaemia v0.8 PARN Louise Daugherty Source NHS GMS was added to PARN.
Cytopenia - NOT Fanconi anaemia v0.8 MPL Louise Daugherty Source NHS GMS was added to MPL.
Cytopenia - NOT Fanconi anaemia v0.8 LIG4 Louise Daugherty Source NHS GMS was added to LIG4.
Cytopenia - NOT Fanconi anaemia v0.8 HOXA11 Louise Daugherty Source NHS GMS was added to HOXA11.
Cytopenia - NOT Fanconi anaemia v0.8 ACD Louise Daugherty Source NHS GMS was added to ACD.
Cytopenia - NOT Fanconi anaemia v0.7 USB1 Louise Daugherty Source London South GLH was added to USB1.
Cytopenia - NOT Fanconi anaemia v0.7 EFL1 Louise Daugherty gene: EFL1 was added
gene: EFL1 was added to Cytopenia - NOT Fanconi anaemia. Sources: London South GLH
Mode of inheritance for gene: EFL1 was set to
Cytopenia - NOT Fanconi anaemia v0.7 JAGN1 Louise Daugherty gene: JAGN1 was added
gene: JAGN1 was added to Cytopenia - NOT Fanconi anaemia. Sources: London South GLH
Mode of inheritance for gene: JAGN1 was set to
Cytopenia - NOT Fanconi anaemia v0.7 VPS45 Louise Daugherty Source London South GLH was added to VPS45.
Cytopenia - NOT Fanconi anaemia v0.7 CSF3R Louise Daugherty Source London South GLH was added to CSF3R.
Cytopenia - NOT Fanconi anaemia v0.7 ETV6 Louise Daugherty gene: ETV6 was added
gene: ETV6 was added to Cytopenia - NOT Fanconi anaemia. Sources: London South GLH
Mode of inheritance for gene: ETV6 was set to
Cytopenia - NOT Fanconi anaemia v0.7 MPIG6B Louise Daugherty Source London South GLH was added to MPIG6B.
Cytopenia - NOT Fanconi anaemia v0.7 THPO Louise Daugherty gene: THPO was added
gene: THPO was added to Cytopenia - NOT Fanconi anaemia. Sources: London South GLH
Mode of inheritance for gene: THPO was set to
Cytopenia - NOT Fanconi anaemia v0.7 SAMD9L Louise Daugherty Source London South GLH was added to SAMD9L.
Cytopenia - NOT Fanconi anaemia v0.7 STIM1 Louise Daugherty gene: STIM1 was added
gene: STIM1 was added to Cytopenia - NOT Fanconi anaemia. Sources: London South GLH
Mode of inheritance for gene: STIM1 was set to
Cytopenia - NOT Fanconi anaemia v0.7 DNAJC21 Louise Daugherty Source London South GLH was added to DNAJC21.
Cytopenia - NOT Fanconi anaemia v0.7 DDX41 Louise Daugherty gene: DDX41 was added
gene: DDX41 was added to Cytopenia - NOT Fanconi anaemia. Sources: London South GLH
Mode of inheritance for gene: DDX41 was set to
Cytopenia - NOT Fanconi anaemia v0.7 ERCC6L2 Louise Daugherty Source London South GLH was added to ERCC6L2.
Cytopenia - NOT Fanconi anaemia v0.7 MECOM Louise Daugherty gene: MECOM was added
gene: MECOM was added to Cytopenia - NOT Fanconi anaemia. Sources: London South GLH
Mode of inheritance for gene: MECOM was set to
Cytopenia - NOT Fanconi anaemia v0.7 SAMD9 Louise Daugherty Source London South GLH was added to SAMD9.
Cytopenia - NOT Fanconi anaemia v0.7 TAZ Louise Daugherty Source London South GLH was added to TAZ.
Cytopenia - NOT Fanconi anaemia v0.7 SLC37A4 Louise Daugherty gene: SLC37A4 was added
gene: SLC37A4 was added to Cytopenia - NOT Fanconi anaemia. Sources: London South GLH
Mode of inheritance for gene: SLC37A4 was set to
Cytopenia - NOT Fanconi anaemia v0.7 HAX1 Louise Daugherty Source London South GLH was added to HAX1.
Cytopenia - NOT Fanconi anaemia v0.7 GFI1 Louise Daugherty Source London South GLH was added to GFI1.
Cytopenia - NOT Fanconi anaemia v0.7 G6PC3 Louise Daugherty Source London South GLH was added to G6PC3.
Cytopenia - NOT Fanconi anaemia v0.7 ELANE Louise Daugherty Source London South GLH was added to ELANE.
Cytopenia - NOT Fanconi anaemia v0.7 CXCR4 Louise Daugherty Source London South GLH was added to CXCR4.
Cytopenia - NOT Fanconi anaemia v0.7 ADA2 Louise Daugherty Source London South GLH was added to ADA2.
Cytopenia - NOT Fanconi anaemia v0.7 ACKR1 Louise Daugherty gene: ACKR1 was added
gene: ACKR1 was added to Cytopenia - NOT Fanconi anaemia. Sources: London South GLH
Mode of inheritance for gene: ACKR1 was set to
Cytopenia - NOT Fanconi anaemia v0.7 WAS Louise Daugherty Source London South GLH was added to WAS.
Cytopenia - NOT Fanconi anaemia v0.7 TUBB1 Louise Daugherty gene: TUBB1 was added
gene: TUBB1 was added to Cytopenia - NOT Fanconi anaemia. Sources: London South GLH
Mode of inheritance for gene: TUBB1 was set to
Cytopenia - NOT Fanconi anaemia v0.7 RBM8A Louise Daugherty gene: RBM8A was added
gene: RBM8A was added to Cytopenia - NOT Fanconi anaemia. Sources: London South GLH
Mode of inheritance for gene: RBM8A was set to
Cytopenia - NOT Fanconi anaemia v0.7 NBEAL2 Louise Daugherty gene: NBEAL2 was added
gene: NBEAL2 was added to Cytopenia - NOT Fanconi anaemia. Sources: London South GLH
Mode of inheritance for gene: NBEAL2 was set to
Cytopenia - NOT Fanconi anaemia v0.7 MYH9 Louise Daugherty gene: MYH9 was added
gene: MYH9 was added to Cytopenia - NOT Fanconi anaemia. Sources: London South GLH
Mode of inheritance for gene: MYH9 was set to
Cytopenia - NOT Fanconi anaemia v0.7 GP1BA Louise Daugherty gene: GP1BA was added
gene: GP1BA was added to Cytopenia - NOT Fanconi anaemia. Sources: London South GLH
Mode of inheritance for gene: GP1BA was set to
Cytopenia - NOT Fanconi anaemia v0.7 ANKRD26 Louise Daugherty gene: ANKRD26 was added
gene: ANKRD26 was added to Cytopenia - NOT Fanconi anaemia. Sources: London South GLH
Mode of inheritance for gene: ANKRD26 was set to
Cytopenia - NOT Fanconi anaemia v0.7 RUNX1 Louise Daugherty gene: RUNX1 was added
gene: RUNX1 was added to Cytopenia - NOT Fanconi anaemia. Sources: London South GLH
Mode of inheritance for gene: RUNX1 was set to
Cytopenia - NOT Fanconi anaemia v0.7 GATA2 Louise Daugherty Source London South GLH was added to GATA2.
Cytopenia - NOT Fanconi anaemia v0.7 WRAP53 Louise Daugherty Source London South GLH was added to WRAP53.
Cytopenia - NOT Fanconi anaemia v0.7 TINF2 Louise Daugherty Source London South GLH was added to TINF2.
Cytopenia - NOT Fanconi anaemia v0.7 TERT Louise Daugherty Source London South GLH was added to TERT.
Cytopenia - NOT Fanconi anaemia v0.7 TERC Louise Daugherty Source London South GLH was added to TERC.
Cytopenia - NOT Fanconi anaemia v0.7 SRP72 Louise Daugherty Source London South GLH was added to SRP72.
Cytopenia - NOT Fanconi anaemia v0.7 SMARCAL1 Louise Daugherty gene: SMARCAL1 was added
gene: SMARCAL1 was added to Cytopenia - NOT Fanconi anaemia. Sources: London South GLH
Mode of inheritance for gene: SMARCAL1 was set to
Cytopenia - NOT Fanconi anaemia v0.7 SBDS Louise Daugherty Source London South GLH was added to SBDS.
Cytopenia - NOT Fanconi anaemia v0.7 RTEL1 Louise Daugherty Source London South GLH was added to RTEL1.
Cytopenia - NOT Fanconi anaemia v0.7 RMRP Louise Daugherty Source London South GLH was added to RMRP.
Cytopenia - NOT Fanconi anaemia v0.7 PARN Louise Daugherty gene: PARN was added
gene: PARN was added to Cytopenia - NOT Fanconi anaemia. Sources: London South GLH
Mode of inheritance for gene: PARN was set to
Cytopenia - NOT Fanconi anaemia v0.7 NOP10 Louise Daugherty Source London South GLH was added to NOP10.
Cytopenia - NOT Fanconi anaemia v0.7 NHP2 Louise Daugherty Source London South GLH was added to NHP2.
Cytopenia - NOT Fanconi anaemia v0.7 MPL Louise Daugherty gene: MPL was added
gene: MPL was added to Cytopenia - NOT Fanconi anaemia. Sources: London South GLH
Mode of inheritance for gene: MPL was set to
Cytopenia - NOT Fanconi anaemia v0.7 MASTL Louise Daugherty Source London South GLH was added to MASTL.
Cytopenia - NOT Fanconi anaemia v0.7 LIG4 Louise Daugherty gene: LIG4 was added
gene: LIG4 was added to Cytopenia - NOT Fanconi anaemia. Sources: London South GLH
Mode of inheritance for gene: LIG4 was set to
Cytopenia - NOT Fanconi anaemia v0.7 HOXA11 Louise Daugherty gene: HOXA11 was added
gene: HOXA11 was added to Cytopenia - NOT Fanconi anaemia. Sources: London South GLH
Mode of inheritance for gene: HOXA11 was set to
Cytopenia - NOT Fanconi anaemia v0.7 DKC1 Louise Daugherty Source London South GLH was added to DKC1.
Cytopenia - NOT Fanconi anaemia v0.7 CTC1 Louise Daugherty Source London South GLH was added to CTC1.
Cytopenia - NOT Fanconi anaemia v0.7 ACD Louise Daugherty gene: ACD was added
gene: ACD was added to Cytopenia - NOT Fanconi anaemia. Sources: London South GLH
Mode of inheritance for gene: ACD was set to
Cytopenia - NOT Fanconi anaemia v0.6 WRAP53 Louise Daugherty reviewed gene: WRAP53: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 WIPF1 Louise Daugherty reviewed gene: WIPF1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 WAS Louise Daugherty reviewed gene: WAS: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 VPS45 Louise Daugherty reviewed gene: VPS45: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 USB1 Louise Daugherty reviewed gene: USB1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 TSR2 Louise Daugherty reviewed gene: TSR2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 TINF2 Louise Daugherty reviewed gene: TINF2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 TERT Louise Daugherty reviewed gene: TERT: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 TERC Louise Daugherty reviewed gene: TERC: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 TAZ Louise Daugherty reviewed gene: TAZ: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 SRP72 Louise Daugherty reviewed gene: SRP72: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 SBDS Louise Daugherty reviewed gene: SBDS: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 SAMD9L Louise Daugherty reviewed gene: SAMD9L: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 SAMD9 Louise Daugherty reviewed gene: SAMD9: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 RTEL1 Louise Daugherty reviewed gene: RTEL1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 RMRP Louise Daugherty reviewed gene: RMRP: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 RPS7 Louise Daugherty reviewed gene: RPS7: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 RPS29 Louise Daugherty reviewed gene: RPS29: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 RPS28 Louise Daugherty reviewed gene: RPS28: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 RPS27 Louise Daugherty reviewed gene: RPS27: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 RPS26 Louise Daugherty reviewed gene: RPS26: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 RPS24 Louise Daugherty reviewed gene: RPS24: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 RPS19 Louise Daugherty reviewed gene: RPS19: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 RPS17 Louise Daugherty reviewed gene: RPS17: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 RPS10 Louise Daugherty reviewed gene: RPS10: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 RPL9 Louise Daugherty reviewed gene: RPL9: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 RPL5 Louise Daugherty reviewed gene: RPL5: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 RPL35A Louise Daugherty reviewed gene: RPL35A: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 RPL31 Louise Daugherty reviewed gene: RPL31: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 RPL27 Louise Daugherty reviewed gene: RPL27: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 RPL26 Louise Daugherty reviewed gene: RPL26: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 RPL18 Louise Daugherty reviewed gene: RPL18: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 RPL15 Louise Daugherty reviewed gene: RPL15: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 RPL11 Louise Daugherty reviewed gene: RPL11: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 RAC2 Louise Daugherty reviewed gene: RAC2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 NOP10 Louise Daugherty reviewed gene: NOP10: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 NHP2 Louise Daugherty reviewed gene: NHP2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 NBN Louise Daugherty reviewed gene: NBN: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 MPIG6B Louise Daugherty reviewed gene: MPIG6B: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 MASTL Louise Daugherty reviewed gene: MASTL: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 LAT Louise Daugherty reviewed gene: LAT: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 KLF1 Louise Daugherty reviewed gene: KLF1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 KIF23 Louise Daugherty reviewed gene: KIF23: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 IKZF1 Louise Daugherty reviewed gene: IKZF1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 HAX1 Louise Daugherty reviewed gene: HAX1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 GFI1 Louise Daugherty reviewed gene: GFI1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 GATA2 Louise Daugherty reviewed gene: GATA2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 GATA1 Louise Daugherty reviewed gene: GATA1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 G6PC3 Louise Daugherty reviewed gene: G6PC3: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 FCGR3B Louise Daugherty reviewed gene: FCGR3B: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 ERCC6L2 Louise Daugherty reviewed gene: ERCC6L2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 ELANE Louise Daugherty reviewed gene: ELANE: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 DNAJC21 Louise Daugherty reviewed gene: DNAJC21: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 DKC1 Louise Daugherty reviewed gene: DKC1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 CXCR4 Louise Daugherty reviewed gene: CXCR4: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 CTC1 Louise Daugherty reviewed gene: CTC1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 CSF3R Louise Daugherty reviewed gene: CSF3R: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.6 ADA2 Louise Daugherty reviewed gene: ADA2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.5 WRAP53 Carl Fratter reviewed gene: WRAP53: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.5 WIPF1 Carl Fratter reviewed gene: WIPF1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.5 WAS Carl Fratter reviewed gene: WAS: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.5 VPS45 Carl Fratter reviewed gene: VPS45: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.5 USB1 Carl Fratter reviewed gene: USB1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.5 TSR2 Carl Fratter reviewed gene: TSR2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.5 TINF2 Carl Fratter reviewed gene: TINF2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.5 TERT Carl Fratter reviewed gene: TERT: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.5 TERC Carl Fratter reviewed gene: TERC: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.5 TAZ Carl Fratter reviewed gene: TAZ: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.5 SRP72 Carl Fratter reviewed gene: SRP72: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.5 SBDS Carl Fratter reviewed gene: SBDS: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.5 SAMD9L Carl Fratter reviewed gene: SAMD9L: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.5 SAMD9 Carl Fratter reviewed gene: SAMD9: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.5 RTEL1 Carl Fratter reviewed gene: RTEL1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.5 RMRP Carl Fratter reviewed gene: RMRP: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.5 RPS7 Carl Fratter reviewed gene: RPS7: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.5 RPS29 Carl Fratter reviewed gene: RPS29: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.5 RPS28 Carl Fratter reviewed gene: RPS28: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.5 RPS27 Carl Fratter reviewed gene: RPS27: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.5 RPS26 Carl Fratter reviewed gene: RPS26: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.5 RPS24 Carl Fratter reviewed gene: RPS24: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.5 RPS19 Carl Fratter reviewed gene: RPS19: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.5 RPS17 Carl Fratter reviewed gene: RPS17: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.5 RPS10 Carl Fratter reviewed gene: RPS10: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.5 RPL9 Carl Fratter reviewed gene: RPL9: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.5 RPL5 Carl Fratter reviewed gene: RPL5: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.5 RPL35A Carl Fratter reviewed gene: RPL35A: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.5 RPL31 Carl Fratter reviewed gene: RPL31: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.5 RPL27 Carl Fratter reviewed gene: RPL27: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.5 RPL26 Carl Fratter reviewed gene: RPL26: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.5 RPL18 Carl Fratter reviewed gene: RPL18: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.5 RPL15 Carl Fratter reviewed gene: RPL15: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.5 RPL11 Carl Fratter reviewed gene: RPL11: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.5 RAC2 Carl Fratter reviewed gene: RAC2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.5 NOP10 Carl Fratter reviewed gene: NOP10: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.5 NHP2 Carl Fratter reviewed gene: NHP2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.5 NBN Carl Fratter reviewed gene: NBN: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.5 MPIG6B Carl Fratter reviewed gene: MPIG6B: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.5 MASTL Carl Fratter reviewed gene: MASTL: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.5 LAT Carl Fratter reviewed gene: LAT: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.5 KLF1 Carl Fratter reviewed gene: KLF1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.5 KIF23 Carl Fratter reviewed gene: KIF23: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.5 IKZF1 Carl Fratter reviewed gene: IKZF1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.5 HAX1 Carl Fratter reviewed gene: HAX1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.5 GFI1 Carl Fratter reviewed gene: GFI1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.5 GATA2 Carl Fratter reviewed gene: GATA2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.5 GATA1 Carl Fratter reviewed gene: GATA1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.5 G6PC3 Carl Fratter reviewed gene: G6PC3: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.5 FCGR3B Carl Fratter reviewed gene: FCGR3B: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.5 ERCC6L2 Carl Fratter reviewed gene: ERCC6L2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.5 ELANE Carl Fratter reviewed gene: ELANE: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.5 DNAJC21 Carl Fratter reviewed gene: DNAJC21: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.5 DKC1 Carl Fratter reviewed gene: DKC1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes
Cytopenia - NOT Fanconi anaemia v0.5 CXCR4 Carl Fratter reviewed gene: CXCR4: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.5 CTC1 Carl Fratter reviewed gene: CTC1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.5 CSF3R Carl Fratter reviewed gene: CSF3R: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.5 ADA2 Carl Fratter reviewed gene: ADA2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Cytopenia - NOT Fanconi anaemia v0.4 WRAP53 Louise Daugherty Source NHS GMS was added to WRAP53.
Cytopenia - NOT Fanconi anaemia v0.4 WIPF1 Louise Daugherty Source NHS GMS was added to WIPF1.
Cytopenia - NOT Fanconi anaemia v0.4 WAS Louise Daugherty Source NHS GMS was added to WAS.
Cytopenia - NOT Fanconi anaemia v0.4 VPS45 Louise Daugherty Source NHS GMS was added to VPS45.
Cytopenia - NOT Fanconi anaemia v0.4 USB1 Louise Daugherty Source NHS GMS was added to USB1.
Cytopenia - NOT Fanconi anaemia v0.4 TSR2 Louise Daugherty Source NHS GMS was added to TSR2.
Cytopenia - NOT Fanconi anaemia v0.4 TINF2 Louise Daugherty Source NHS GMS was added to TINF2.
Cytopenia - NOT Fanconi anaemia v0.4 TERT Louise Daugherty Source NHS GMS was added to TERT.
Cytopenia - NOT Fanconi anaemia v0.4 TERC Louise Daugherty Source NHS GMS was added to TERC.
Cytopenia - NOT Fanconi anaemia v0.4 TAZ Louise Daugherty Source NHS GMS was added to TAZ.
Cytopenia - NOT Fanconi anaemia v0.4 SRP72 Louise Daugherty Source NHS GMS was added to SRP72.
Cytopenia - NOT Fanconi anaemia v0.4 SBDS Louise Daugherty Source NHS GMS was added to SBDS.
Cytopenia - NOT Fanconi anaemia v0.4 SAMD9L Louise Daugherty Source NHS GMS was added to SAMD9L.
Cytopenia - NOT Fanconi anaemia v0.4 SAMD9 Louise Daugherty Source NHS GMS was added to SAMD9.
Cytopenia - NOT Fanconi anaemia v0.4 RTEL1 Louise Daugherty Source NHS GMS was added to RTEL1.
Cytopenia - NOT Fanconi anaemia v0.4 RMRP Louise Daugherty Source NHS GMS was added to RMRP.
Cytopenia - NOT Fanconi anaemia v0.4 RPS7 Louise Daugherty Source NHS GMS was added to RPS7.
Cytopenia - NOT Fanconi anaemia v0.4 RPS29 Louise Daugherty Source NHS GMS was added to RPS29.
Cytopenia - NOT Fanconi anaemia v0.4 RPS28 Louise Daugherty Source NHS GMS was added to RPS28.
Cytopenia - NOT Fanconi anaemia v0.4 RPS27 Louise Daugherty Source NHS GMS was added to RPS27.
Cytopenia - NOT Fanconi anaemia v0.4 RPS26 Louise Daugherty Source NHS GMS was added to RPS26.
Cytopenia - NOT Fanconi anaemia v0.4 RPS24 Louise Daugherty Source NHS GMS was added to RPS24.
Cytopenia - NOT Fanconi anaemia v0.4 RPS19 Louise Daugherty Source NHS GMS was added to RPS19.
Cytopenia - NOT Fanconi anaemia v0.4 RPS17 Louise Daugherty Source NHS GMS was added to RPS17.
Cytopenia - NOT Fanconi anaemia v0.4 RPS10 Louise Daugherty Source NHS GMS was added to RPS10.
Cytopenia - NOT Fanconi anaemia v0.4 RPL9 Louise Daugherty Source NHS GMS was added to RPL9.
Cytopenia - NOT Fanconi anaemia v0.4 RPL5 Louise Daugherty Source NHS GMS was added to RPL5.
Cytopenia - NOT Fanconi anaemia v0.4 RPL35A Louise Daugherty Source NHS GMS was added to RPL35A.
Cytopenia - NOT Fanconi anaemia v0.4 RPL31 Louise Daugherty Source NHS GMS was added to RPL31.
Cytopenia - NOT Fanconi anaemia v0.4 RPL27 Louise Daugherty Source NHS GMS was added to RPL27.
Cytopenia - NOT Fanconi anaemia v0.4 RPL26 Louise Daugherty Source NHS GMS was added to RPL26.
Cytopenia - NOT Fanconi anaemia v0.4 RPL18 Louise Daugherty Source NHS GMS was added to RPL18.
Cytopenia - NOT Fanconi anaemia v0.4 RPL15 Louise Daugherty Source NHS GMS was added to RPL15.
Cytopenia - NOT Fanconi anaemia v0.4 RPL11 Louise Daugherty Source NHS GMS was added to RPL11.
Cytopenia - NOT Fanconi anaemia v0.4 RAC2 Louise Daugherty Source NHS GMS was added to RAC2.
Cytopenia - NOT Fanconi anaemia v0.4 NOP10 Louise Daugherty Source NHS GMS was added to NOP10.
Cytopenia - NOT Fanconi anaemia v0.4 NHP2 Louise Daugherty Source NHS GMS was added to NHP2.
Cytopenia - NOT Fanconi anaemia v0.4 NBN Louise Daugherty Source NHS GMS was added to NBN.
Cytopenia - NOT Fanconi anaemia v0.4 MPIG6B Louise Daugherty Source NHS GMS was added to MPIG6B.
Cytopenia - NOT Fanconi anaemia v0.4 MASTL Louise Daugherty Source NHS GMS was added to MASTL.
Cytopenia - NOT Fanconi anaemia v0.4 LAT Louise Daugherty Source NHS GMS was added to LAT.
Cytopenia - NOT Fanconi anaemia v0.4 KLF1 Louise Daugherty Source NHS GMS was added to KLF1.
Cytopenia - NOT Fanconi anaemia v0.4 KIF23 Louise Daugherty Source NHS GMS was added to KIF23.
Cytopenia - NOT Fanconi anaemia v0.4 IKZF1 Louise Daugherty Source NHS GMS was added to IKZF1.
Cytopenia - NOT Fanconi anaemia v0.4 HAX1 Louise Daugherty Source NHS GMS was added to HAX1.
Cytopenia - NOT Fanconi anaemia v0.4 GFI1 Louise Daugherty Source NHS GMS was added to GFI1.
Cytopenia - NOT Fanconi anaemia v0.4 GATA2 Louise Daugherty Source NHS GMS was added to GATA2.
Cytopenia - NOT Fanconi anaemia v0.4 GATA1 Louise Daugherty Source NHS GMS was added to GATA1.
Cytopenia - NOT Fanconi anaemia v0.4 G6PC3 Louise Daugherty Source NHS GMS was added to G6PC3.
Cytopenia - NOT Fanconi anaemia v0.4 FCGR3B Louise Daugherty Source NHS GMS was added to FCGR3B.
Cytopenia - NOT Fanconi anaemia v0.4 ERCC6L2 Louise Daugherty Source NHS GMS was added to ERCC6L2.
Cytopenia - NOT Fanconi anaemia v0.4 ELANE Louise Daugherty Source NHS GMS was added to ELANE.
Cytopenia - NOT Fanconi anaemia v0.4 DNAJC21 Louise Daugherty Source NHS GMS was added to DNAJC21.
Cytopenia - NOT Fanconi anaemia v0.4 DKC1 Louise Daugherty Source NHS GMS was added to DKC1.
Cytopenia - NOT Fanconi anaemia v0.4 CXCR4 Louise Daugherty Source NHS GMS was added to CXCR4.
Cytopenia - NOT Fanconi anaemia v0.4 CTC1 Louise Daugherty Source NHS GMS was added to CTC1.
Cytopenia - NOT Fanconi anaemia v0.4 CSF3R Louise Daugherty Source NHS GMS was added to CSF3R.
Cytopenia - NOT Fanconi anaemia v0.4 ADA2 Louise Daugherty Source NHS GMS was added to ADA2.
Cytopenia - NOT Fanconi anaemia v0.3 WRAP53 Louise Daugherty Source Expert Review Amber was added to WRAP53.
Mode of inheritance for gene WRAP53 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Dyskeratosis Congenita, Autosomal Recessive, 3; Dyskeratosis Congenita, Recessive; Inherited Bone Marrow Failure Syndromes; Dyskeratosis congenita, autosomal recessive 3, 613988; Dyskeratosis congenita for gene: WRAP53
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.3 WIPF1 Louise Daugherty Source Expert Review Green was added to WIPF1.
Mode of inheritance for gene WIPF1 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes WIP deficiency; Wiskott-Aldrich syndrome like, WIP deficiency; Thrombocytopenia with or without small platelets, recurrent bacterial and viral infections, eczema, bloody diarrhea, WAS protein absent; ?Wiskott-Aldrich syndrome 2, 614493 for gene: WIPF1
Publications for gene WIPF1 were changed from to 27742395; 11869681; 22231303; 14757742; 9405671
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 WAS Louise Daugherty Source Expert Review Green was added to WAS.
Mode of inheritance for gene WAS was changed from to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Added phenotypes Thrombocytopenia, X-linked 313900; Thrombocytopenia, X-linked, intermittent, 313900; Wiskott-Aldrich syndrome, 301000; Neutropenia, severe congenital, X-linked, 300299 for gene: WAS
Publications for gene WAS were changed from to 16804117
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 VPS45 Louise Daugherty Source Expert Review Green was added to VPS45.
Mode of inheritance for gene VPS45 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Congenital neutropenia-bone marrow fibrosis-nephromegaly syndrome; Neutropenia, severe congenital, 5, autosomal recessive, 615285; Severe congenital neutropenia; VPS45 deficiency for gene: VPS45
Publications for gene VPS45 were changed from to 23738510; 23599270
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 USB1 Louise Daugherty Source Expert Review Amber was added to USB1.
Added phenotypes Poikiloderma with neutropenia, 604173; Dyskeratosis congenita for gene: USB1
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.3 TSR2 Louise Daugherty Source Expert Review Amber was added to TSR2.
Mode of inheritance for gene TSR2 was changed from to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Added phenotypes ?Diamond-Blackfan anemia 14 with mandibulofacial dysostosis, 300946 for gene: TSR2
Publications for gene TSR2 were changed from to 24942156; 20301769
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.3 TINF2 Louise Daugherty Source Expert Review Amber was added to TINF2.
Mode of inheritance for gene TINF2 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Added phenotypes Inherited Bone Marrow Failure Syndromes - Aplastic Anaemia; Revesz Syndrome; Dyskeratosis Congenita, Autosomal Dominant, 3; DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 3; Dyskeratosis congenita; Dyskeratosis congenita, autosomal dominant 3, 613990; Revesz syndrome, 268130; Inherited Bone Marrow Failure Syndromes; Dyskeratosis Congenita, Dominant for gene: TINF2
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.3 TERT Louise Daugherty Source Expert Review Green was added to TERT.
Mode of inheritance for gene TERT was changed from to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Added phenotypes {Pulmonary fibrosis, telomere-related, 1}, 614742; {Dyskeratosis congenita, autosomal dominant 2}, 613989; Coronary artery disease; {Melanoma, cutaneous malignant, 9}, 615134; Aplastic Anemia; {Leukemia, acute myeloid}, 601626; {Dyskeratosis congenita, autosomal recessive 4}, 613989 for gene: TERT
Publications for gene TERT were changed from to 15885610; 19179534; 15814878
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 TERC Louise Daugherty Source Expert Review Amber was added to TERC.
Mode of inheritance for gene TERC was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Added phenotypes Inherited Bone Marrow Failure Syndromes - Aplastic Anaemia; Telomere_Related Pulmonary Fibrosis And/Or Bone Marrow Failure_1; Telomere_Related Pulmonary Fibrosis And/Or Bone Marrow Failure_2; DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1; Dyskeratosis congenita; Dyskeratosis Congenita, Autosomal Dominant, 1; Inherited Bone Marrow Failure Syndromes for gene: TERC
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.3 TAZ Louise Daugherty Source Expert Review Green was added to TAZ.
Mode of inheritance for gene TAZ was changed from to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Added phenotypes Barth syndrome, 302060 for gene: TAZ
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 SRP72 Louise Daugherty Source Expert Review Amber was added to SRP72.
Mode of inheritance for gene SRP72 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Added phenotypes Inherited Bone Marrow Failure Syndromes - Aplastic Anaemia; Familial Bone Marrow Failure; Bone Marrow Failure, Familial; Bone marrow failure, familial, 614675; Familial MDS (Myelodysplastic syndromes) for gene: SRP72
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.3 SBDS Louise Daugherty Source Expert Review Green was added to SBDS.
Mode of inheritance for gene SBDS was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Shwachman-Diamond syndrome 260400 for gene: SBDS
Publications for gene SBDS were changed from to 14749921; 12496757
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 SAMD9L Louise Daugherty Source Expert Review Green was added to SAMD9L.
Mode of inheritance for gene SAMD9L was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Added phenotypes Ataxia-pancytopenia syndrome, 159550 for gene: SAMD9L
Publications for gene SAMD9L were changed from to 27259050; 28202457
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 SAMD9 Louise Daugherty Source Expert Review Green was added to SAMD9.
Mode of inheritance for gene SAMD9 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Added phenotypes MIRAGE syndrome, 617053 for gene: SAMD9
Publications for gene SAMD9 were changed from to 27182967
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 RTEL1 Louise Daugherty Source Expert Review Green was added to RTEL1.
Mode of inheritance for gene RTEL1 was changed from to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Added phenotypes Dyskeratosis congenita, autosomal recessive 5 615190; Dyskeratosis congenita, autosomal dominant 4, 615190 for gene: RTEL1
Publications for gene RTEL1 were changed from to 23591994; 23453664; 23329068
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 RMRP Louise Daugherty Source Expert Review Green was added to RMRP.
Mode of inheritance for gene RMRP was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Cartilage-hair hypoplasia; Severe congenital neutropenia for gene: RMRP
Publications for gene RMRP were changed from to 11207361
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 RPS7 Louise Daugherty Source Expert Review Green was added to RPS7.
Mode of inheritance for gene RPS7 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Added phenotypes DIAMOND-BLACKFAN ANEMIA 8; Diamond_Blackfan Anemia 8; Diamond-Blackfan anemia 8, 612563; Diamond-Blackfan Anemia; Inherited Bone Marrow Failure Syndromes; Diamond Blackfan anemia for gene: RPS7
Publications for gene RPS7 were changed from to 25946618; 23718193; 27882484; 19061985
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 RPS29 Louise Daugherty Source Expert Review Green was added to RPS29.
Mode of inheritance for gene RPS29 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Added phenotypes Diamond-Blackfan anemia 13 615909 for gene: RPS29
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 RPS28 Louise Daugherty Source Expert Review Amber was added to RPS28.
Mode of inheritance for gene RPS28 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Added phenotypes Diamond Blackfan anemia 15 with mandibulofacial dysostosis, 606164 for gene: RPS28
Publications for gene RPS28 were changed from to 24942156; 20301769
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.3 RPS27 Louise Daugherty Source Expert Review Green was added to RPS27.
Mode of inheritance for gene RPS27 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Added phenotypes Diamond-Blackfan anemia; ?Diamond-Blackfan anemia 17, 617409 for gene: RPS27
Publications for gene RPS27 were changed from to 23718193; 25424902
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 RPS26 Louise Daugherty Source Expert Review Green was added to RPS26.
Mode of inheritance for gene RPS26 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Added phenotypes Diamond_Blackfan Anemia 10; Diamond-Blackfan anemia 10, 613309; Diamond-Blackfan anemia 10; Diamond-Blackfan Anemia; Inherited Bone Marrow Failure Syndromes; Diamond Blackfan anemia for gene: RPS26
Publications for gene RPS26 were changed from to 24675553; 25946618; 24942156; 20116044
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 RPS24 Louise Daugherty Source Expert Review Green was added to RPS24.
Mode of inheritance for gene RPS24 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Added phenotypes Diamond_Blackfan Anemia 3; DIAMOND-BLACKFAN ANEMIA 3; Diamond-Blackfan Anemia; Inherited Bone Marrow Failure Syndromes; Diamond-blackfan anemia 3, 610629; Diamond Blackfan anemia for gene: RPS24
Publications for gene RPS24 were changed from to 17186470; 19689926; 19773262; 25946618; 8647458; 2210388
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 RPS19 Louise Daugherty Source Expert Review Green was added to RPS19.
Mode of inheritance for gene RPS19 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Added phenotypes Diamond_Blackfan Anemia; Diamond-Blackfan anemia 1, 105650; DIAMOND-BLACKFAN ANEMIA 1; Diamond-Blackfan Anemia; Inherited Bone Marrow Failure Syndromes; Diamond Blackfan anemia for gene: RPS19
Publications for gene RPS19 were changed from to 25946618; 24675553; 15384984; 9988267
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 RPS17 Louise Daugherty Source Expert Review Green was added to RPS17.
Mode of inheritance for gene RPS17 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Added phenotypes Diamond-Blackfan anemia 4, 612527 for gene: RPS17
Publications for gene RPS17 were changed from to 22045982; 19953637; 17647292; 19061985
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 RPS10 Louise Daugherty Source Expert Review Green was added to RPS10.
Mode of inheritance for gene RPS10 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Added phenotypes Inherited Bone Marrow Failure Syndromes; Diamond_Blackfan Anemia 9; Diamond-Blackfan Anemia; Diamond-Blackfan anemia 9, 613308; DIAMOND-BLACKFAN ANEMIA 9; Diamond Blackfan anemia for gene: RPS10
Publications for gene RPS10 were changed from to 25946618; 20116044; 23718193
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 RPL9 Louise Daugherty Source Expert Review Green was added to RPL9.
Mode of inheritance for gene RPL9 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Added phenotypes Diamond-Blackfan anemia for gene: RPL9
Publications for gene RPL9 were changed from to 23718193; 20116044
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 RPL5 Louise Daugherty Source Expert Review Green was added to RPL5.
Mode of inheritance for gene RPL5 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Added phenotypes Diamond-Blackfan anemia 6, 612561; DIAMOND-BLACKFAN ANEMIA 6; Diamond_Blackfan Anemia 6; Diamond-Blackfan Anemia; Inherited Bone Marrow Failure Syndromes; Diamond Blackfan anemia for gene: RPL5
Publications for gene RPL5 were changed from to 25946618; 19191325; 19061985
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 RPL35A Louise Daugherty Source Expert Review Green was added to RPL35A.
Mode of inheritance for gene RPL35A was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Added phenotypes Diamond-Blackfan anemia 5, 612528; Diamond-Blackfan Anemia; DIAMOND-BLACKFAN ANEMIA 5; Inherited Bone Marrow Failure Syndromes; Diamond_Blackfan Anemia 5; Diamond Blackfan anemia for gene: RPL35A
Publications for gene RPL35A were changed from to 25946618; 18535205
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 RPL31 Louise Daugherty Source Expert Review Green was added to RPL31.
Mode of inheritance for gene RPL31 was changed from to Unknown
Publications for gene RPL31 were changed from to 25424902; 25042156
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 RPL27 Louise Daugherty Source Expert Review Green was added to RPL27.
Mode of inheritance for gene RPL27 was changed from to Unknown
Added phenotypes Diamond-Blackfan anemia; ?Diamond-Blackfan anemia 16, 617408 for gene: RPL27
Publications for gene RPL27 were changed from to 25424902
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 RPL26 Louise Daugherty Source Expert Review Green was added to RPL26.
Mode of inheritance for gene RPL26 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Added phenotypes ?Diamond-Blackfan anemia 11,614900 for gene: RPL26
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 RPL18 Louise Daugherty Source Expert Review Amber was added to RPL18.
Mode of inheritance for gene RPL18 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Added phenotypes Diamond-Blackfan anaemia for gene: RPL18
Publications for gene RPL18 were changed from to 28280134
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.3 RPL15 Louise Daugherty Source Expert Review Green was added to RPL15.
Mode of inheritance for gene RPL15 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Added phenotypes ?Diamond-Blackfan anemia 12, 615550 for gene: RPL15
Publications for gene RPL15 were changed from to 23812780; 19438500
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 RPL11 Louise Daugherty Source Expert Review Green was added to RPL11.
Mode of inheritance for gene RPL11 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Added phenotypes Diamond_Blackfan Anemia 7; Diamond-Blackfan Anemia; DIAMOND-BLACKFAN ANEMIA 7; Diamond-Blackfan anemia 7, 612562; Inherited Bone Marrow Failure Syndromes; Diamond Blackfan anemia for gene: RPL11
Publications for gene RPL11 were changed from to 19191325; 19061985
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 RAC2 Louise Daugherty Source Expert Review Amber was added to RAC2.
Added phenotypes Neutrophil immunodeficiency syndrome, 608203 for gene: RAC2
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.3 NOP10 Louise Daugherty Source Expert Review Amber was added to NOP10.
Mode of inheritance for gene NOP10 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Dyskeratosis congenita, autosomal recessive 1, 224230 for gene: NOP10
Publications for gene NOP10 were changed from to 17507419
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.3 NHP2 Louise Daugherty Source Expert Review Amber was added to NHP2.
Mode of inheritance for gene NHP2 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Dyskeratosis congenita, autosomal recessive 2,613987 for gene: NHP2
Publications for gene NHP2 were changed from to 18523010
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.3 NBN Louise Daugherty Source Expert Review Green was added to NBN.
Mode of inheritance for gene NBN was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Aplastic anemia, 609135; Leukemia, acute lymphoblastic, 613065; Nijmegen breakage syndrome, 251260 for gene: NBN
Publications for gene NBN were changed from to 15338273; 11325820
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 MPIG6B Louise Daugherty Source Expert Review Amber was added to MPIG6B.
Mode of inheritance for gene MPIG6B was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes ?Thrombocytopenia, anemia, and myelofibrosis, 617441 for gene: MPIG6B
Publications for gene MPIG6B were changed from to 27743390
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.3 MASTL Louise Daugherty Source Expert Review Amber was added to MASTL.
Mode of inheritance for gene MASTL was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Added phenotypes severe aplastic anemia; Thrombocytopenia for gene: MASTL
Publications for gene MASTL were changed from to 12890928; 26136524; 21211618
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.3 LAT Louise Daugherty Source Expert Review Amber was added to LAT.
Mode of inheritance for gene LAT was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Immunodeficiency 52, 617514 for gene: LAT
Publications for gene LAT were changed from to 27522155; 27242165
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.3 KLF1 Louise Daugherty Source Expert Review Green was added to KLF1.
Mode of inheritance for gene KLF1 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Added phenotypes Dyserythropoietic anemia, congenital, type IV, 613673; Congenital Dyserythropoietic Anemia for gene: KLF1
Publications for gene KLF1 were changed from to 21055716
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 KIF23 Louise Daugherty Source Expert Review Green was added to KIF23.
Mode of inheritance for gene KIF23 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Added phenotypes CDA III; Congenital dyserythropoietic anemia (CDA); Congenital dyserythropoietic anemia type III; Enzyme Disorder for gene: KIF23
Publications for gene KIF23 were changed from to 7711721; 7323912; 23570799
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 IKZF1 Louise Daugherty Source Expert Review Amber was added to IKZF1.
Mode of inheritance for gene IKZF1 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Added phenotypes Acute lymphoblastic leukemia (ALL); Immunodeficiency, common variable, 13,616873 for gene: IKZF1
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.3 HAX1 Louise Daugherty Source Expert Review Green was added to HAX1.
Mode of inheritance for gene HAX1 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Neutropenia, severe congenital 3, autosomal recessive, 610738; Inherited Bone Marrow Failure Syndromes - Neutropenia; Severe congenital neutropenic; Neutropenia, Severe Congenital, 3 Autosomal Dominant for gene: HAX1
Publications for gene HAX1 were changed from to 17187068; 10581030; 18024606; 18337561
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 GFI1 Louise Daugherty Source Expert Review Green was added to GFI1.
Mode of inheritance for gene GFI1 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Added phenotypes Neutropenia, Nonimmune Chronic Idiopathic, Of Adults; Inherited Bone Marrow Failure Syndromes - Neutropenia; Neutropenia, Severe Congenital, 2 Autosomal Dominant; Severe congenital neutropenic; Neutropenia, severe congenital 2, autosomal dominant, 613107 for gene: GFI1
Publications for gene GFI1 were changed from to 12530980; 12778173; 11810106; 19775295
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 GATA2 Louise Daugherty Source Expert Review Green was added to GATA2.
Mode of inheritance for gene GATA2 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Added phenotypes Congenital dyserythropoietic anemia (CDA); Myelodysplastic Syndrome; Familial MDS (Myelodysplastic syndromes); Leukemia, Acute Myeloid; {Leukemia, acute myeloid, susceptibility to}, 601626; Inherited Bone Marrow Failure Syndromes - GATA2 deficiencies; {Myelodysplastic syndrome, susceptibility to}, 614286; Primary Lymphedema with Myelodysplasia; Lymphedema, Primary, With Myelodysplasia; Dendritic Cell, Monocyte, B Lymphocyte, And Natural Killer Lymphocyte Deficiency; Immunodeficiency 21; Emberger syndrome, 614038 (includes pancytopenia); Dendritic cell, monocyte, B lymphocyte, and natural killer lymphocyte deficiency, 614172 for gene: GATA2
Publications for gene GATA2 were changed from to 27418648; 21892162
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 GATA1 Louise Daugherty Source Expert Review Green was added to GATA1.
Mode of inheritance for gene GATA1 was changed from to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Added phenotypes Diamond Blackfan Anaemia; Thrombocytopenia, X-linked, with or without dyserythropoietic anemia, 300367; Anemia, X-linked, with/without neutropenia and/or platelet abnormalities, 300835; Myelodysplastic syndrome (MDS), Paediatric for gene: GATA1
Publications for gene GATA1 were changed from to 22706301; 24952648; 24766296; 10700180; 24453067
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 G6PC3 Louise Daugherty Source Expert Review Green was added to G6PC3.
Mode of inheritance for gene G6PC3 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Dursun syndrome, 612541; Severe congenital neutropenic; Inherited Bone Marrow Failure Syndromes - Neutropenia; Neutropenia, severe congenital 4, autosomal recessive, 612541; Neutropenia, Severe Congenital, 4 Autosomal Dominant; Severe Congenital Neutropenia for gene: G6PC3
Publications for gene G6PC3 were changed from to 19118303
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 FCGR3B Louise Daugherty Source Expert Review Amber was added to FCGR3B.
Mode of inheritance for gene FCGR3B was changed from to Other - please specify in evaluation comments
Added phenotypes Neutropenia,alloimmuneneonatal for gene: FCGR3B
Rating Changed from Red List (low evidence) to Amber List (moderate evidence)
Cytopenia - NOT Fanconi anaemia v0.3 ERCC6L2 Louise Daugherty Source Expert Review Green was added to ERCC6L2.
Mode of inheritance for gene ERCC6L2 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Bone marrow failure syndrome 2, 615715 for gene: ERCC6L2
Publications for gene ERCC6L2 were changed from to 24507776; 27185855
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 ELANE Louise Daugherty Source Expert Review Green was added to ELANE.
Mode of inheritance for gene ELANE was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Added phenotypes Neutropenia, cyclic 162800; Neutropenia, severe congenital 1, autosomal dominant 202700 for gene: ELANE
Publications for gene ELANE were changed from to 10581030; 11675333
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 DNAJC21 Louise Daugherty Source Expert Review Green was added to DNAJC21.
Mode of inheritance for gene DNAJC21 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Pancytopaenia; Bone Marrow Failure; Bone marrow failure syndrome 3, 617052 for gene: DNAJC21
Publications for gene DNAJC21 were changed from to 27346687; 29700810; 28062395
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 DKC1 Louise Daugherty Source Expert Review Green was added to DKC1.
Mode of inheritance for gene DKC1 was changed from to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Added phenotypes Dyskeratosis congenita, X-linked, 305000; Dyskeratosis congenita for gene: DKC1
Publications for gene DKC1 were changed from to 10583221; 9590285; 9590276; 10217077
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 CXCR4 Louise Daugherty Source Expert Review Green was added to CXCR4.
Mode of inheritance for gene CXCR4 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Added phenotypes Warts, hypogammaglobulinemia, infections, and myelokathexis, Myelokathexis, isolated; WHIM syndrome, 193670; Severe congenital neutropenia for gene: CXCR4
Publications for gene CXCR4 were changed from to 12692554; 15536153
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 CTC1 Louise Daugherty Source Expert Review Green was added to CTC1.
Mode of inheritance for gene CTC1 was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Cerebroretinal microangiopathy with calcifications and cysts/CTC1 related Dyskeratosis Congenita; Dyskeratosis Congenita, Recessive; Inherited Bone Marrow Failure Syndromes; Dyskeratosis congenita for gene: CTC1
Publications for gene CTC1 were changed from to 22532422; 22899577
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 CSF3R Louise Daugherty Source Expert Review Green was added to CSF3R.
Mode of inheritance for gene CSF3R was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Neutropenia, severe congenital, 7, autosomal recessive, 617014; Severe congenital neutropenia for gene: CSF3R
Publications for gene CSF3R were changed from to 26324699; 24753537; 9001427
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.3 ADA2 Louise Daugherty Source Expert Review Green was added to ADA2.
Added phenotypes Diamond Blackfan anaemia for gene: ADA2
Rating Changed from Red List (low evidence) to Green List (high evidence)
Cytopenia - NOT Fanconi anaemia v0.2 WRAP53 Louise Daugherty gene: WRAP53 was added
gene: WRAP53 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: WRAP53 was set to
Cytopenia - NOT Fanconi anaemia v0.2 WIPF1 Louise Daugherty gene: WIPF1 was added
gene: WIPF1 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: WIPF1 was set to
Cytopenia - NOT Fanconi anaemia v0.2 WAS Louise Daugherty gene: WAS was added
gene: WAS was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: WAS was set to
Cytopenia - NOT Fanconi anaemia v0.2 VPS45 Louise Daugherty gene: VPS45 was added
gene: VPS45 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: VPS45 was set to
Cytopenia - NOT Fanconi anaemia v0.2 USB1 Louise Daugherty gene: USB1 was added
gene: USB1 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: USB1 was set to
Cytopenia - NOT Fanconi anaemia v0.2 TSR2 Louise Daugherty gene: TSR2 was added
gene: TSR2 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: TSR2 was set to
Cytopenia - NOT Fanconi anaemia v0.2 TINF2 Louise Daugherty gene: TINF2 was added
gene: TINF2 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: TINF2 was set to
Cytopenia - NOT Fanconi anaemia v0.2 TERT Louise Daugherty gene: TERT was added
gene: TERT was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: TERT was set to
Cytopenia - NOT Fanconi anaemia v0.2 TERC Louise Daugherty gene: TERC was added
gene: TERC was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: TERC was set to
Cytopenia - NOT Fanconi anaemia v0.2 TAZ Louise Daugherty gene: TAZ was added
gene: TAZ was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: TAZ was set to
Cytopenia - NOT Fanconi anaemia v0.2 SRP72 Louise Daugherty gene: SRP72 was added
gene: SRP72 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: SRP72 was set to
Cytopenia - NOT Fanconi anaemia v0.2 SBDS Louise Daugherty gene: SBDS was added
gene: SBDS was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: SBDS was set to
Cytopenia - NOT Fanconi anaemia v0.2 SAMD9L Louise Daugherty gene: SAMD9L was added
gene: SAMD9L was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: SAMD9L was set to
Cytopenia - NOT Fanconi anaemia v0.2 SAMD9 Louise Daugherty gene: SAMD9 was added
gene: SAMD9 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: SAMD9 was set to
Cytopenia - NOT Fanconi anaemia v0.2 RTEL1 Louise Daugherty gene: RTEL1 was added
gene: RTEL1 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: RTEL1 was set to
Cytopenia - NOT Fanconi anaemia v0.2 RMRP Louise Daugherty gene: RMRP was added
gene: RMRP was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: RMRP was set to
Cytopenia - NOT Fanconi anaemia v0.2 RPS7 Louise Daugherty gene: RPS7 was added
gene: RPS7 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: RPS7 was set to
Cytopenia - NOT Fanconi anaemia v0.2 RPS29 Louise Daugherty gene: RPS29 was added
gene: RPS29 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: RPS29 was set to
Cytopenia - NOT Fanconi anaemia v0.2 RPS28 Louise Daugherty gene: RPS28 was added
gene: RPS28 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: RPS28 was set to
Cytopenia - NOT Fanconi anaemia v0.2 RPS27 Louise Daugherty gene: RPS27 was added
gene: RPS27 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: RPS27 was set to
Cytopenia - NOT Fanconi anaemia v0.2 RPS26 Louise Daugherty gene: RPS26 was added
gene: RPS26 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: RPS26 was set to
Cytopenia - NOT Fanconi anaemia v0.2 RPS24 Louise Daugherty gene: RPS24 was added
gene: RPS24 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: RPS24 was set to
Cytopenia - NOT Fanconi anaemia v0.2 RPS19 Louise Daugherty gene: RPS19 was added
gene: RPS19 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: RPS19 was set to
Cytopenia - NOT Fanconi anaemia v0.2 RPS17 Louise Daugherty gene: RPS17 was added
gene: RPS17 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: RPS17 was set to
Cytopenia - NOT Fanconi anaemia v0.2 RPS10 Louise Daugherty gene: RPS10 was added
gene: RPS10 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: RPS10 was set to
Cytopenia - NOT Fanconi anaemia v0.2 RPL9 Louise Daugherty gene: RPL9 was added
gene: RPL9 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: RPL9 was set to
Cytopenia - NOT Fanconi anaemia v0.2 RPL5 Louise Daugherty gene: RPL5 was added
gene: RPL5 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: RPL5 was set to
Cytopenia - NOT Fanconi anaemia v0.2 RPL35A Louise Daugherty gene: RPL35A was added
gene: RPL35A was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: RPL35A was set to
Cytopenia - NOT Fanconi anaemia v0.2 RPL31 Louise Daugherty gene: RPL31 was added
gene: RPL31 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: RPL31 was set to
Cytopenia - NOT Fanconi anaemia v0.2 RPL27 Louise Daugherty gene: RPL27 was added
gene: RPL27 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: RPL27 was set to
Cytopenia - NOT Fanconi anaemia v0.2 RPL26 Louise Daugherty gene: RPL26 was added
gene: RPL26 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: RPL26 was set to
Cytopenia - NOT Fanconi anaemia v0.2 RPL18 Louise Daugherty gene: RPL18 was added
gene: RPL18 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: RPL18 was set to
Cytopenia - NOT Fanconi anaemia v0.2 RPL15 Louise Daugherty gene: RPL15 was added
gene: RPL15 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: RPL15 was set to
Cytopenia - NOT Fanconi anaemia v0.2 RPL11 Louise Daugherty gene: RPL11 was added
gene: RPL11 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: RPL11 was set to
Cytopenia - NOT Fanconi anaemia v0.2 RAC2 Louise Daugherty gene: RAC2 was added
gene: RAC2 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: RAC2 was set to
Cytopenia - NOT Fanconi anaemia v0.2 NOP10 Louise Daugherty gene: NOP10 was added
gene: NOP10 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: NOP10 was set to
Cytopenia - NOT Fanconi anaemia v0.2 NHP2 Louise Daugherty gene: NHP2 was added
gene: NHP2 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: NHP2 was set to
Cytopenia - NOT Fanconi anaemia v0.2 NBN Louise Daugherty gene: NBN was added
gene: NBN was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: NBN was set to
Cytopenia - NOT Fanconi anaemia v0.2 MPIG6B Louise Daugherty gene: MPIG6B was added
gene: MPIG6B was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: MPIG6B was set to
Cytopenia - NOT Fanconi anaemia v0.2 MASTL Louise Daugherty gene: MASTL was added
gene: MASTL was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: MASTL was set to
Cytopenia - NOT Fanconi anaemia v0.2 LAT Louise Daugherty gene: LAT was added
gene: LAT was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: LAT was set to
Cytopenia - NOT Fanconi anaemia v0.2 KLF1 Louise Daugherty gene: KLF1 was added
gene: KLF1 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: KLF1 was set to
Cytopenia - NOT Fanconi anaemia v0.2 KIF23 Louise Daugherty gene: KIF23 was added
gene: KIF23 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: KIF23 was set to
Cytopenia - NOT Fanconi anaemia v0.2 IKZF1 Louise Daugherty gene: IKZF1 was added
gene: IKZF1 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: IKZF1 was set to
Cytopenia - NOT Fanconi anaemia v0.2 HAX1 Louise Daugherty gene: HAX1 was added
gene: HAX1 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: HAX1 was set to
Cytopenia - NOT Fanconi anaemia v0.2 GFI1 Louise Daugherty gene: GFI1 was added
gene: GFI1 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: GFI1 was set to
Cytopenia - NOT Fanconi anaemia v0.2 GATA2 Louise Daugherty gene: GATA2 was added
gene: GATA2 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: GATA2 was set to
Cytopenia - NOT Fanconi anaemia v0.2 GATA1 Louise Daugherty gene: GATA1 was added
gene: GATA1 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: GATA1 was set to
Cytopenia - NOT Fanconi anaemia v0.2 G6PC3 Louise Daugherty gene: G6PC3 was added
gene: G6PC3 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: G6PC3 was set to
Cytopenia - NOT Fanconi anaemia v0.2 FCGR3B Louise Daugherty gene: FCGR3B was added
gene: FCGR3B was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: FCGR3B was set to
Cytopenia - NOT Fanconi anaemia v0.2 ERCC6L2 Louise Daugherty gene: ERCC6L2 was added
gene: ERCC6L2 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: ERCC6L2 was set to
Cytopenia - NOT Fanconi anaemia v0.2 ELANE Louise Daugherty gene: ELANE was added
gene: ELANE was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: ELANE was set to
Cytopenia - NOT Fanconi anaemia v0.2 DNAJC21 Louise Daugherty gene: DNAJC21 was added
gene: DNAJC21 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: DNAJC21 was set to
Cytopenia - NOT Fanconi anaemia v0.2 DKC1 Louise Daugherty gene: DKC1 was added
gene: DKC1 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: DKC1 was set to
Cytopenia - NOT Fanconi anaemia v0.2 CXCR4 Louise Daugherty gene: CXCR4 was added
gene: CXCR4 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: CXCR4 was set to
Cytopenia - NOT Fanconi anaemia v0.2 CTC1 Louise Daugherty gene: CTC1 was added
gene: CTC1 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: CTC1 was set to
Cytopenia - NOT Fanconi anaemia v0.2 CSF3R Louise Daugherty gene: CSF3R was added
gene: CSF3R was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: CSF3R was set to
Cytopenia - NOT Fanconi anaemia v0.2 ADA2 Louise Daugherty gene: ADA2 was added
gene: ADA2 was added to Cytopenia - NOT Fanconi anaemia. Sources: Wessex and West Midlands GLH
Mode of inheritance for gene: ADA2 was set to
Cytopenia - NOT Fanconi anaemia v0.0 Ellen McDonagh Added Panel Cytopenia - NOT Fanconi anaemia
Set panel types to: GMS Rare Disease