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Congenital Heart Defect v0.55 BCOR Zornitza Stark Marked gene: BCOR as ready
Congenital Heart Defect v0.55 BCOR Zornitza Stark Gene: bcor has been classified as Green List (High Evidence).
Congenital Heart Defect v0.55 BCOR Zornitza Stark Phenotypes for gene: BCOR were changed from to Microphthalmia, syndromic 2, MIM# 300166; Oculofaciocardiodental syndrome; Lenz microphthalmia
Congenital Heart Defect v0.54 BCOR Zornitza Stark Publications for gene: BCOR were set to
Congenital Heart Defect v0.53 BCOR Zornitza Stark Mode of inheritance for gene: BCOR was changed from Unknown to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Congenital Heart Defect v0.52 BCOR Zornitza Stark reviewed gene: BCOR: Rating: GREEN; Mode of pathogenicity: None; Publications: 29974297; Phenotypes: Microphthalmia, syndromic 2, MIM# 300166, Oculofaciocardiodental syndrome, Lenz microphthalmia; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Congenital Heart Defect v0.0 BCOR Zornitza Stark gene: BCOR was added
gene: BCOR was added to Congenital Heart Defect_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: BCOR was set to Unknown