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Mendeliome v0.13729 CRBN Ain Roesley Marked gene: CRBN as ready
Mendeliome v0.13729 CRBN Ain Roesley Gene: crbn has been classified as Amber List (Moderate Evidence).
Mendeliome v0.13729 CRBN Ain Roesley Phenotypes for gene: CRBN were changed from to Intellectual developmental disorder, autosomal recessive 2 MIM#607417
Mendeliome v0.13728 CRBN Ain Roesley Mode of inheritance for gene: CRBN was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendeliome v0.13729 CRBN Ain Roesley Publications for gene: CRBN were set to
Mendeliome v0.13728 CRBN Ain Roesley Classified gene: CRBN as Amber List (moderate evidence)
Mendeliome v0.13728 CRBN Ain Roesley Gene: crbn has been classified as Amber List (Moderate Evidence).
Mendeliome v0.13727 CRBN Ain Roesley reviewed gene: CRBN: Rating: AMBER; Mode of pathogenicity: None; Publications: 15557513, 28143899; Phenotypes: Intellectual developmental disorder, autosomal recessive 2 MIM#607417; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Mendeliome v0.0 CRBN Zornitza Stark gene: CRBN was added
gene: CRBN was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: CRBN was set to Unknown