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Congenital Disorders of Glycosylation v0.351 SEC23B Zornitza Stark Marked gene: SEC23B as ready
Congenital Disorders of Glycosylation v0.351 SEC23B Zornitza Stark Gene: sec23b has been classified as Green List (High Evidence).
Congenital Disorders of Glycosylation v0.351 SEC23B Zornitza Stark Phenotypes for gene: SEC23B were changed from to Dyserythropoietic anemia, congenital, type II 224100; COPII component SEC23B (Disorders of multiple glycosylation and other glycosylation pathways, V-ATPase deficiencies)
Congenital Disorders of Glycosylation v0.350 SEC23B Zornitza Stark Publications for gene: SEC23B were set to
Congenital Disorders of Glycosylation v0.349 SEC23B Zornitza Stark Mode of inheritance for gene: SEC23B was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Congenital Disorders of Glycosylation v0.348 SEC23B Zornitza Stark reviewed gene: SEC23B: Rating: GREEN; Mode of pathogenicity: None; Publications: 19561605, 19621418; Phenotypes: Dyserythropoietic anemia, congenital, type II 224100, COPII component SEC23B (Disorders of multiple glycosylation and other glycosylation pathways, V-ATPase deficiencies); Mode of inheritance: None
Congenital Disorders of Glycosylation v0.0 SEC23B Zornitza Stark gene: SEC23B was added
gene: SEC23B was added to Congenital Disorders of Glycosylation_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: SEC23B was set to Unknown