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Retinitis pigmentosa_Autosomal Dominant v0.23 SEMA4A Zornitza Stark Tag refuted tag was added to gene: SEMA4A.
Retinitis pigmentosa_Autosomal Dominant v0.23 SEMA4A Zornitza Stark Marked gene: SEMA4A as ready
Retinitis pigmentosa_Autosomal Dominant v0.23 SEMA4A Zornitza Stark Gene: sema4a has been classified as Red List (Low Evidence).
Retinitis pigmentosa_Autosomal Dominant v0.23 SEMA4A Zornitza Stark Publications for gene: SEMA4A were set to
Retinitis pigmentosa_Autosomal Dominant v0.22 SEMA4A Zornitza Stark Mode of inheritance for gene: SEMA4A was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Retinitis pigmentosa_Autosomal Dominant v0.21 SEMA4A Zornitza Stark Classified gene: SEMA4A as Red List (low evidence)
Retinitis pigmentosa_Autosomal Dominant v0.21 SEMA4A Zornitza Stark Gene: sema4a has been classified as Red List (Low Evidence).
Retinitis pigmentosa_Autosomal Dominant v0.20 SEMA4A Zornitza Stark reviewed gene: SEMA4A: Rating: RED; Mode of pathogenicity: None; Publications: 16199541, 28805479, 23360997, 15277503; Phenotypes: Retinitis pigmentosa 35, MIM# 610282; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Retinitis pigmentosa_Autosomal Dominant v0.0 SEMA4A Bryony Thompson gene: SEMA4A was added
gene: SEMA4A was added to Autosomal Dominant Retinitis Pigmentosa_RMH. Sources: Royal Melbourne Hospital,Expert Review Green
Mode of inheritance for gene: SEMA4A was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes for gene: SEMA4A were set to Cone-rod dystrophy 10, 610283; Retinitis pigmentosa 35, 610282