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Intellectual disability syndromic and non-syndromic v0.1029 PRX Zornitza Stark Marked gene: PRX as ready
Intellectual disability syndromic and non-syndromic v0.1029 PRX Zornitza Stark Gene: prx has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.1029 PRX Zornitza Stark Phenotypes for gene: PRX were changed from to Charcot-Marie-Tooth disease, type 4F, MIM#614895
Intellectual disability syndromic and non-syndromic v0.1028 PRX Zornitza Stark Mode of inheritance for gene: PRX was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.1027 PRX Zornitza Stark Classified gene: PRX as Red List (low evidence)
Intellectual disability syndromic and non-syndromic v0.1027 PRX Zornitza Stark Gene: prx has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.1026 PRX Zornitza Stark reviewed gene: PRX: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Charcot-Marie-Tooth disease, type 4F, MIM#614895; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.0 PRX Zornitza Stark gene: PRX was added
gene: PRX was added to Intellectual disability, syndromic and non-syndromic_GHQ. Sources: Expert Review Green,Genetic Health Queensland
Mode of inheritance for gene: PRX was set to Unknown