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Structural eye disease v3.79 ALX1 Arina Puzriakova Tag Q3_23_promote_green was removed from gene: ALX1.
Tag Q3_23_NHS_review was removed from gene: ALX1.
Structural eye disease v3.79 ALX1 Arina Puzriakova reviewed gene: ALX1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Structural eye disease v3.78 ALX1 Arina Puzriakova Source Expert Review Green was added to ALX1.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Structural eye disease v3.21 ALX1 Sarah Leigh Tag Q3_23_promote_green tag was added to gene: ALX1.
Tag Q3_23_NHS_review tag was added to gene: ALX1.
Structural eye disease v3.21 ALX1 Sarah Leigh Classified gene: ALX1 as Amber List (moderate evidence)
Structural eye disease v3.21 ALX1 Sarah Leigh Added comment: Comment on list classification: There is enough evidence for this gene to be rated GREEN at the next major review.
Structural eye disease v3.21 ALX1 Sarah Leigh Gene: alx1 has been classified as Amber List (Moderate Evidence).
Structural eye disease v3.20 ALX1 Sarah Leigh reviewed gene: ALX1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
Structural eye disease v3.20 ALX1 Sarah Leigh Publications for gene: ALX1 were set to 20451171; 23059813; 32914578; 27324866; 32914578
Structural eye disease v3.19 ALX1 Sarah Leigh Publications for gene: ALX1 were set to 20451171; 23059813; 32914578; 27324866
Structural eye disease v3.18 ALX1 Sarah Leigh Publications for gene: ALX1 were set to 20451171; 23059813; 32914578
Structural eye disease v3.17 ALX1 Sarah Leigh Deleted their review
Structural eye disease v3.17 ALX1 Sarah Leigh Deleted their comment
Structural eye disease v3.17 ALX1 Sarah Leigh Added comment: Comment on phenotypes: Frontonasal dysplasia 3, OMIM:613456;frontonasal dysplasia - severe microphthalmia - severe facial clefting syndrome, MONDO:0013271
Structural eye disease v3.17 ALX1 Sarah Leigh Phenotypes for gene: ALX1 were changed from Frontonasal Dysplasia 3, FND3, 613456 to Frontonasal dysplasia 3, OMIM:613456; frontonasal dysplasia - severe microphthalmia - severe facial clefting syndrome, MONDO:0013271
Structural eye disease v3.16 ALX1 Sarah Leigh Publications for gene: ALX1 were set to 20451171; 23059813
Structural eye disease v3.4 ALX1 Hannah Knight reviewed gene: ALX1: Rating: GREEN; Mode of pathogenicity: None; Publications: 32914578; Phenotypes: Frontonasal Dysplasia 3; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Structural eye disease v0.91 ALX1 Nicola Ragge reviewed gene: ALX1: Rating: AMBER; Mode of pathogenicity: ; Publications: 20451171, 23059813; Phenotypes: ; Mode of inheritance:
Structural eye disease v0.89 ALX1 Ivone Leong Source NHS GMS was added to ALX1.
Publications for gene ALX1 were changed from to 20451171; 23059813
Structural eye disease v0.87 ALX1 Ivone Leong Classified gene: ALX1 as Amber List (moderate evidence)
Structural eye disease v0.87 ALX1 Ivone Leong Gene: alx1 has been classified as Amber List (Moderate Evidence).
Structural eye disease v0.60 ALX1 Mariya Moosajee reviewed gene: ALX1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Frontonasal Dysplasia 3, FND3; Mode of inheritance:
Structural eye disease v0.59 ALX1 Ivone Leong gene: ALX1 was added
gene: ALX1 was added to Structural eye disease. Sources: London North GLH
Mode of inheritance for gene: ALX1 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: ALX1 were set to Frontonasal Dysplasia 3, FND3, 613456