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Mendeliome v0.13739 CRYGB Ain Roesley Marked gene: CRYGB as ready
Mendeliome v0.13739 CRYGB Ain Roesley Gene: crygb has been classified as Red List (Low Evidence).
Mendeliome v0.13739 CRYGB Ain Roesley Phenotypes for gene: CRYGB were changed from to Cataract 39, multiple types, autosomal dominant MIM#615188
Mendeliome v0.13738 CRYGB Ain Roesley Mode of inheritance for gene: CRYGB was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.13739 CRYGB Ain Roesley Publications for gene: CRYGB were set to
Mendeliome v0.13738 CRYGB Ain Roesley Classified gene: CRYGB as Red List (low evidence)
Mendeliome v0.13738 CRYGB Ain Roesley Gene: crygb has been classified as Red List (Low Evidence).
Mendeliome v0.13737 CRYGB Ain Roesley reviewed gene: CRYGB: Rating: RED; Mode of pathogenicity: None; Publications: 23288985; Phenotypes: Cataract 39, multiple types, autosomal dominant MIM#615188; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes
Mendeliome v0.0 CRYGB Zornitza Stark gene: CRYGB was added
gene: CRYGB was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: CRYGB was set to Unknown