Activity

Filter

Cancel
Date Panel Item Activity
15 actions
Brugada syndrome v0.33 GPD1L Zornitza Stark Publications for gene: GPD1L were set to 17967977; 19666841
Brugada syndrome v0.32 GPD1L Zornitza Stark Classified gene: GPD1L as Red List (low evidence)
Brugada syndrome v0.32 GPD1L Zornitza Stark Gene: gpd1l has been classified as Red List (Low Evidence).
Brugada syndrome v0.13 GPD1L Ivan Macciocca reviewed gene: GPD1L: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 29959160; Phenotypes: ; Mode of inheritance: None
Brugada syndrome v0.10 GPD1L Zornitza Stark Marked gene: GPD1L as ready
Brugada syndrome v0.10 GPD1L Zornitza Stark Added comment: Comment when marking as ready: Rated as DISPUTED by ClinGen.
Brugada syndrome v0.10 GPD1L Zornitza Stark Gene: gpd1l has been classified as Amber List (Moderate Evidence).
Brugada syndrome v0.10 GPD1L Zornitza Stark Phenotypes for gene: GPD1L were changed from to Brugada syndrome 2, MIM# 611777
Brugada syndrome v0.9 GPD1L Zornitza Stark Publications for gene: GPD1L were set to
Brugada syndrome v0.8 GPD1L Zornitza Stark Mode of inheritance for gene: GPD1L was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Brugada syndrome v0.7 GPD1L Zornitza Stark Tag disputed tag was added to gene: GPD1L.
Brugada syndrome v0.7 GPD1L Zornitza Stark Classified gene: GPD1L as Amber List (moderate evidence)
Brugada syndrome v0.7 GPD1L Zornitza Stark Gene: gpd1l has been classified as Amber List (Moderate Evidence).
Brugada syndrome v0.6 GPD1L Elena Savva reviewed gene: GPD1L: Rating: AMBER; Mode of pathogenicity: None; Publications: PMID: 17967977, 19666841; Phenotypes: Brugada syndrome 2 611777; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Brugada syndrome v0.0 GPD1L Zornitza Stark gene: GPD1L was added
gene: GPD1L was added to Brugada syndrome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: GPD1L was set to Unknown