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Arthrogryposis v0.432 ASXL1 Zornitza Stark Marked gene: ASXL1 as ready
Arthrogryposis v0.432 ASXL1 Zornitza Stark Gene: asxl1 has been classified as Green List (High Evidence).
Arthrogryposis v0.432 ASXL1 Zornitza Stark Phenotypes for gene: ASXL1 were changed from to Bohring-Opitz syndrome , MIM#605039
Arthrogryposis v0.431 ASXL1 Zornitza Stark Mode of inheritance for gene: ASXL1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Arthrogryposis v0.430 ASXL1 Zornitza Stark changed review comment from: Well established gene-disease association. Arthrogryposis is key feature.; to: Well established gene-disease association. Contractures are a key feature.
Arthrogryposis v0.430 ASXL1 Zornitza Stark reviewed gene: ASXL1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Bohring-Opitz syndrome , MIM#605039; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Arthrogryposis v0.0 ASXL1 Zornitza Stark gene: ASXL1 was added
gene: ASXL1 was added to Arthrogryposis_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: ASXL1 was set to Unknown