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Intellectual disability syndromic and non-syndromic v0.874 NOP10 Zornitza Stark Marked gene: NOP10 as ready
Intellectual disability syndromic and non-syndromic v0.874 NOP10 Zornitza Stark Gene: nop10 has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.874 NOP10 Zornitza Stark Phenotypes for gene: NOP10 were changed from to Dyskeratosis congenita, autosomal recessive 1, MIM#224230
Intellectual disability syndromic and non-syndromic v0.873 NOP10 Zornitza Stark Publications for gene: NOP10 were set to
Intellectual disability syndromic and non-syndromic v0.872 NOP10 Zornitza Stark Mode of inheritance for gene: NOP10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.871 NOP10 Zornitza Stark Classified gene: NOP10 as Red List (low evidence)
Intellectual disability syndromic and non-syndromic v0.871 NOP10 Zornitza Stark Gene: nop10 has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.870 NOP10 Zornitza Stark reviewed gene: NOP10: Rating: RED; Mode of pathogenicity: None; Publications: 17507419; Phenotypes: Dyskeratosis congenita, autosomal recessive 1, MIM#224230; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.0 NOP10 Zornitza Stark gene: NOP10 was added
gene: NOP10 was added to Intellectual disability, syndromic and non-syndromic_GHQ. Sources: Expert Review Green,Genetic Health Queensland
Mode of inheritance for gene: NOP10 was set to Unknown