Activity
|
|
Retinal disorders v1.191
|
TPP1
|
Catherine Snow Mode of inheritance for gene: TPP1 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal
|
|
|
Retinal disorders v1.190
|
TPP1
|
Catherine Snow Phenotypes for gene: TPP1 were changed from Eye Disorders to Eye Disorders; Ceroid lipofuscinosis, neuronal, 2, 204500
|
|
|
Retinal disorders v1.189
|
TPP1
|
Catherine Snow Mode of inheritance for gene: TPP1 was changed from to BIALLELIC, autosomal or pseudoautosomal
|
|
|
Retinal disorders v1.188
|
TPP1
|
Catherine Snow Classified gene: TPP1 as Green List (high evidence)
|
|
|
Retinal disorders v1.188
|
TPP1
|
Catherine Snow Gene: tpp1 has been classified as Green List (High Evidence).
|
|
|
Retinal disorders v1.187
|
TPP1
|
Catherine Snow reviewed gene: TPP1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Ceroid lipofuscinosis, neuronal, 2, 204500; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
|
|
|
Retinal disorders v1.159
|
TPP1
|
Gavin Arno reviewed gene: TPP1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
|
|
|
Retinal disorders v1.137
|
TPP1
|
Ivone Leong Source NHS GMS was added to TPP1.
|