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Skeletal dysplasia v4.20 FGF9 Eleanor Williams Tag Q2_23_promote_green was removed from gene: FGF9.
Skeletal dysplasia v4.20 FGF9 Eleanor Williams edited their review of gene: FGF9: Added comment: The rating of this gene has been updated to green following NHS Genomic Medicine Service approval.; Changed rating: GREEN; Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Skeletal dysplasia v4.19 FGF9 Eleanor Williams Source Expert Review Green was added to FGF9.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Skeletal dysplasia v4.10 FGF9 Eleanor Williams Phenotypes for gene: FGF9 were changed from ?Multiple synostoses syndrome type 3 612961 to Multiple synostoses syndrome 3, OMIM:612961; multiple synostoses syndrome 3, MONDO:0013064
Skeletal dysplasia v4.9 FGF9 Eleanor Williams Publications for gene: FGF9 were set to 19589401
Skeletal dysplasia v4.8 FGF9 Eleanor Williams Classified gene: FGF9 as Amber List (moderate evidence)
Skeletal dysplasia v4.8 FGF9 Eleanor Williams Added comment: Comment on list classification: Promoting this gene from red to amber but with a recommendation for GREEN rating following GMS review as 4 unrelated cases with variants in FGF9 and a phenotype of multiple synostoses syndrome.
Skeletal dysplasia v4.8 FGF9 Eleanor Williams Gene: fgf9 has been classified as Amber List (Moderate Evidence).
Skeletal dysplasia v4.7 FGF9 Eleanor Williams Tag watchlist was removed from gene: FGF9.
Tag Q2_23_promote_green tag was added to gene: FGF9.
Skeletal dysplasia v2.80 FGF9 Zornitza Stark edited their review of gene: FGF9: Set current diagnostic: yes
Skeletal dysplasia v2.80 FGF9 Zornitza Stark reviewed gene: FGF9: Rating: GREEN; Mode of pathogenicity: None; Publications: 33140402, 28730625, 19589401, 33174625; Phenotypes: Multiple synostoses syndrome 3, OMIM # 612961; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Skeletal dysplasia v1.153 FGF9 Eleanor Williams Added phenotypes ?Multiple synostoses syndrome type 3 612961 for gene: FGF9
Skeletal dysplasia v1.147 FGF9 Tracy Lester reviewed gene: FGF9: Rating: AMBER; Mode of pathogenicity: ; Publications: 19589401; Phenotypes: ?Multiple synostoses syndrome type 3 612961; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Skeletal dysplasia v1.146 FGF9 Eleanor Williams reviewed gene: FGF9: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Skeletal dysplasia v1.145 FGF9 Eleanor Williams Source NHS GMS was added to FGF9.
Skeletal dysplasia FGF9 Sarah Leigh edited their review of FGF9
Skeletal dysplasia FGF9 Sarah Leigh classified FGF9 as red