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Combined Immunodeficiency v0.5 NOP10 Zornitza Stark Marked gene: NOP10 as ready
Combined Immunodeficiency v0.5 NOP10 Zornitza Stark Gene: nop10 has been classified as Red List (Low Evidence).
Combined Immunodeficiency v0.5 NOP10 Zornitza Stark Mode of inheritance for gene: NOP10 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal
Combined Immunodeficiency v0.4 NOP10 Zornitza Stark Phenotypes for gene: NOP10 were changed from to Dyskeratosis congenita, autosomal recessive 1, MIM#224230
Combined Immunodeficiency v0.4 NOP10 Zornitza Stark Mode of inheritance for gene: NOP10 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Combined Immunodeficiency v0.4 NOP10 Zornitza Stark Publications for gene: NOP10 were set to
Combined Immunodeficiency v0.3 NOP10 Zornitza Stark Classified gene: NOP10 as Red List (low evidence)
Combined Immunodeficiency v0.3 NOP10 Zornitza Stark Gene: nop10 has been classified as Red List (Low Evidence).
Combined Immunodeficiency v0.0 NOP10 Zornitza Stark gene: NOP10 was added
gene: NOP10 was added to Combined immunodeficiency_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship
Mode of inheritance for gene: NOP10 was set to Unknown