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Predominantly Antibody Deficiency v0.102 INO80 Zornitza Stark Marked gene: INO80 as ready
Predominantly Antibody Deficiency v0.102 INO80 Zornitza Stark Gene: ino80 has been classified as Amber List (Moderate Evidence).
Predominantly Antibody Deficiency v0.102 INO80 Zornitza Stark Phenotypes for gene: INO80 were changed from to Primary immunodeficiency, MONDO:0003778
Predominantly Antibody Deficiency v0.101 INO80 Zornitza Stark Publications for gene: INO80 were set to
Predominantly Antibody Deficiency v0.100 INO80 Zornitza Stark Mode of inheritance for gene: INO80 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Predominantly Antibody Deficiency v0.99 INO80 Zornitza Stark Classified gene: INO80 as Amber List (moderate evidence)
Predominantly Antibody Deficiency v0.99 INO80 Zornitza Stark Gene: ino80 has been classified as Amber List (Moderate Evidence).
Predominantly Antibody Deficiency v0.98 INO80 Zornitza Stark reviewed gene: INO80: Rating: AMBER; Mode of pathogenicity: None; Publications: 25312759; Phenotypes: Primary immunodeficiency, MONDO:0003778; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Predominantly Antibody Deficiency v0.0 INO80 Zornitza Stark gene: INO80 was added
gene: INO80 was added to Predominantly antibody deficiency_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship
Mode of inheritance for gene: INO80 was set to Unknown