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Cholestasis v2.0 CFTR Gene migrated from ENSG00000001626 to ENSG00000001626 (gene set migration)
Cholestasis v1.12 CFTR Zornitza Stark Publications for gene: CFTR were set to 25097709
Cholestasis v1.11 CFTR Zornitza Stark Classified gene: CFTR as Green List (high evidence)
Cholestasis v1.11 CFTR Zornitza Stark Gene: cftr has been classified as Green List (High Evidence).
Cholestasis v1.11 CFTR Zornitza Stark Classified gene: CFTR as Green List (high evidence)
Cholestasis v1.11 CFTR Zornitza Stark Gene: cftr has been classified as Green List (High Evidence).
Cholestasis v1.10 CFTR Freeman A reviewed gene: CFTR: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 8813874, 3967446, 22798282, 27806795, 23949094, 24436365, 34510112.; Phenotypes: cholestasis; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cholestasis v0.53 CFTR Zornitza Stark Marked gene: CFTR as ready
Cholestasis v0.53 CFTR Zornitza Stark Gene: cftr has been classified as Amber List (Moderate Evidence).
Cholestasis v0.53 CFTR Zornitza Stark Phenotypes for gene: CFTR were changed from to Cystic fibrosis, MIM# 219700
Cholestasis v0.52 CFTR Zornitza Stark Publications for gene: CFTR were set to
Cholestasis v0.51 CFTR Zornitza Stark Mode of inheritance for gene: CFTR was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Cholestasis v0.50 CFTR Zornitza Stark Classified gene: CFTR as Amber List (moderate evidence)
Cholestasis v0.50 CFTR Zornitza Stark Gene: cftr has been classified as Amber List (Moderate Evidence).
Cholestasis v0.49 CFTR Zornitza Stark reviewed gene: CFTR: Rating: AMBER; Mode of pathogenicity: None; Publications: 25097709; Phenotypes: Cystic fibrosis, MIM# 219700; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cholestasis v0.0 CFTR Zornitza Stark gene: CFTR was added
gene: CFTR was added to Cholestasis_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: CFTR was set to Unknown