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Retinitis pigmentosa_Autosomal Dominant v0.57 PRPF4 Sangavi Sivagnanasundram reviewed gene: PRPF4: Rating: GREEN; Mode of pathogenicity: None; Publications: 24419317; Phenotypes: inherited retinal dystrophy MONDO:0019118; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Retinitis pigmentosa_Autosomal Dominant v0.44 PRPF4 Zornitza Stark Marked gene: PRPF4 as ready
Retinitis pigmentosa_Autosomal Dominant v0.44 PRPF4 Zornitza Stark Gene: prpf4 has been classified as Green List (High Evidence).
Retinitis pigmentosa_Autosomal Dominant v0.44 PRPF4 Zornitza Stark Phenotypes for gene: PRPF4 were changed from Retinitis pigmentosa 70 to Retinitis pigmentosa 70, MIM# 615922
Retinitis pigmentosa_Autosomal Dominant v0.43 PRPF4 Zornitza Stark Publications for gene: PRPF4 were set to
Retinitis pigmentosa_Autosomal Dominant v0.42 PRPF4 Zornitza Stark Mode of inheritance for gene: PRPF4 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Retinitis pigmentosa_Autosomal Dominant v0.41 PRPF4 Zornitza Stark reviewed gene: PRPF4: Rating: GREEN; Mode of pathogenicity: None; Publications: 24419317, 25383878; Phenotypes: Retinitis pigmentosa 70, MIM# 615922; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Retinitis pigmentosa_Autosomal Dominant v0.0 PRPF4 Bryony Thompson gene: PRPF4 was added
gene: PRPF4 was added to Autosomal Dominant Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green
Mode of inheritance for gene: PRPF4 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes for gene: PRPF4 were set to Retinitis pigmentosa 70