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Chromosome Breakage Disorders v0.82 FANCA Zornitza Stark changed review comment from: Well established gene-disease association.; to: Well established gene-disease association.

Fanconi anaemia causes genomic instability and is characterised by multiple congenital anomalies including radial ray abnormalities and microcephaly, early-onset bone marrow failure, and a predisposition to cancer.
Chromosome Breakage Disorders v0.82 FANCA Zornitza Stark Marked gene: FANCA as ready
Chromosome Breakage Disorders v0.82 FANCA Zornitza Stark Gene: fanca has been classified as Green List (High Evidence).
Chromosome Breakage Disorders v0.82 FANCA Zornitza Stark Phenotypes for gene: FANCA were changed from to Fanconi anaemia, complementation group A, MIM# 227650; MONDO:0009215
Chromosome Breakage Disorders v0.81 FANCA Zornitza Stark Publications for gene: FANCA were set to
Chromosome Breakage Disorders v0.80 FANCA Zornitza Stark Mode of inheritance for gene: FANCA was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Chromosome Breakage Disorders v0.79 FANCA Zornitza Stark reviewed gene: FANCA: Rating: GREEN; Mode of pathogenicity: None; Publications: 10094191; Phenotypes: Fanconi anaemia, complementation group A, MIM# 227650, MONDO:0009215; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Chromosome Breakage Disorders v0.2 FANCA Zornitza Stark gene: FANCA was added
gene: FANCA was added to Chromosome breakage disorders_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: FANCA was set to Unknown