- Panels
- Newborns main panel
- FANCE
- AAAS 1
- ABCB11 1
- ABCB4 1
- ABCC6 1
- ABCC8 2
- ABCD1 1
- ABCD4 1
- ACAD9 1
- ACADM 1
- ACADVL 2
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- ERCC6L2 1
- F11 1
- FANCA 1
- FANCB 1
- FANCC 1
- FANCD2 1
- FANCE 1
- FANCF 1
- FANCG 1
- FANCI 1
- FANCL 1
- FARS2 1
- FGFR3 1
- FOXA2 1
- FOXI1 1
- FUCA1 1
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- G6PD 1
- GALC 1
- GALM 1
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- GATA2 1
- GATA4 1
- GATA6 1
- GBA 2
- GCH1 1
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- GLA 1
- GLRA1 1
- GLRB 1
- GLRX5 1
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- GOT2 1
- GRIN2A 1
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- HAMP 1
- HAVCR2 1
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- HBA2 2
- HCFC1 1
- HFE2 1
- HGD 1
- HIBCH 1
- HMBS 1
- HNF1A 1
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- HOXA11 1
- HSCB 1
- HSPA9 1
- IARS 1
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- IFIH1 1
- IGFALS 1
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- IL1RN 1
- IL21 1
- IL21R 1
- IL36RN 1
- INSR 1
- IRF2BP2 1
- JAK1 1
- KCNA1 1
- KCNE1 1
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- KCNQ1 2
- KCNQ2 3
- KCNT1 2
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- KDSR 1
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- SCN2A 3
- SCN3A 1
- SCN5A 2
- SCN8A 3
- SERPINA1 1
- SERPING1 2
- SFTPC 1
- SLC13A5 1
- SLC16A1 1
- SLC16A2 1
- SLC18A2 1
- SLC1A3 1
- SLC25A38 1
- SLC26A3 2
- SLC26A4 1
- SLC2A2 1
- SLC35A2 1
- SLC35C1 1
- SLC39A14 1
- SLC39A8 1
- SLC40A1 1
- SLC4A4 1
- SLC5A6 1
- SLC6A5 1
- SLC6A6 1
- SLC6A8 1
- SLC9A3 2
- SLX4 1
- SMARCA4 1
- SMARCB1 1
- SMPD1 1
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- HNF4A 1
- KL 1
- KLF11 1
- MUTYH 1
- NF1 1
- PKD1 1
- PKD2 1
- SCARB2 1
- SLC12A3 1
- SLC30A2 1
- SMAD4 1
- TNFRSF13B 1
- UCP2 1
- WDR72 1
- WFS1 1
Newborns main panel
Gene: FANCE Amber List (moderate evidence)EnsemblGeneIds (GRCh38): ENSG00000112039
EnsemblGeneIds (GRCh37): ENSG00000112039
OMIM: 613976, Gene2Phenotype
FANCE is in 20 panels
1 review
Mafalda Gomes (Genomics England Curator)
The mechanism of pathogenicity is loss-of-function (LOF).Created: 1 Jun 2023, 2:40 p.m. | Last Modified: 1 Jun 2023, 2:40 p.m.
Panel Version: 0.137
FANCE curation results (clinicalgenome.org)Created: 1 Jun 2023, 12:22 p.m. | Last Modified: 1 Jun 2023, 12:22 p.m.
Panel Version: 0.134
Last Modified: 1 Jun 2023, 12:22 p.m.
Panel version: 0.137
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Amber
- Phenotypes
-
- Fanconi anemia, complementation group E
- OMIM
- 613976
- Clinvar variants
- Variants in FANCE
- Penetrance
- None
- Panels with this gene
-
- Childhood solid tumours cancer susceptibility
- Radial dysplasia
- Haematological malignancies cancer susceptibility
- Cytopenias and congenital anaemias
- Severe microcephaly
- COVID-19 research
- Limb disorders
- Structural eye disease
- Monogenic short stature
- Neurofibromatosis Type 1
- Childhood solid tumours
- Haematological malignancies for rare disease
- Intellectual disability
- Confirmed Fanconi anaemia or Bloom syndrome
- Pigmentary skin disorders
- Head and neck cancer pertinent cancer susceptibility
- Adult solid tumours cancer susceptibility
- IUGR and IGF abnormalities
- Fetal anomalies
- DDG2P
History Filter Activity
Added New Source, Set Phenotypes, Status Update
Mafalda Gomes (Genomics England Curator)Source Expert Review Amber was added to FANCE. Added phenotypes Fanconi anemia, complementation group E for gene: FANCE Rating Changed from Green List (high evidence) to Amber List (moderate evidence)
Set Phenotypes
Mafalda Gomes (Genomics England Curator)Added phenotypes Fanconi anemia, complementation group E for gene: FANCE
Set Phenotypes
Mafalda Gomes (Genomics England Curator)Added phenotypes Fanconi anemia, complementation group E for gene: FANCE
Added New Source, Set Phenotypes, Status Update
Mafalda Gomes (Genomics England Curator)Source Expert Review Green was added to FANCE. Added phenotypes Fanconi anemia, complementation group E for gene: FANCE Rating Changed from No List (delete) to Green List (high evidence)
Added New Source, Status Update
Mafalda Gomes (Genomics England Curator)Source Expert Review Removed was added to FANCE. Rating Changed from Green List (high evidence) to No List (delete)
Set Phenotypes
Mafalda Gomes (Genomics England Curator)Added phenotypes Fanconi anemia, complementation group E for gene: FANCE
Created, Added New Source, Set mode of inheritance
Mafalda Gomes (Genomics England Curator)gene: FANCE was added gene: FANCE was added to Newborns main panel. Sources: Expert Review Green Mode of inheritance for gene: FANCE was set to BIALLELIC, autosomal or pseudoautosomal