Activity

Filter

Cancel
Date Panel Item Activity
9 actions
Polydactyly v0.120 PROM1 Zornitza Stark Marked gene: PROM1 as ready
Polydactyly v0.120 PROM1 Zornitza Stark Gene: prom1 has been classified as Red List (Low Evidence).
Polydactyly v0.120 PROM1 Zornitza Stark Phenotypes for gene: PROM1 were changed from to Cone-rod dystrophy 12, MIM# 612657; Macular dystrophy, retinal, 2, MIM# 608051; Retinitis pigmentosa 41, MIM# 612095; Stargardt disease 4, MIM# 603786
Polydactyly v0.119 PROM1 Zornitza Stark Classified gene: PROM1 as Red List (low evidence)
Polydactyly v0.119 PROM1 Zornitza Stark Gene: prom1 has been classified as Red List (Low Evidence).
Polydactyly v0.118 PROM1 Zornitza Stark reviewed gene: PROM1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Cone-rod dystrophy 12, MIM# 612657, Macular dystrophy, retinal, 2, MIM# 608051, Retinitis pigmentosa 41, MIM# 612095, Stargardt disease 4, MIM# 603786; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Polydactyly v0.118 PROM1 Zornitza Stark Mode of inheritance for gene: PROM1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Polydactyly v0.36 PROM1 Anand Vasudevan reviewed gene: PROM1: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Polydactyly v0.0 PROM1 Zornitza Stark gene: PROM1 was added
gene: PROM1 was added to Polydactyly_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: PROM1 was set to Unknown