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Brain Channelopathies v2.0 CACNB4 Gene migrated from ENSG00000182389 to ENSG00000182389 (gene set migration)
Brain Channelopathies v0.66 CACNB4 Zornitza Stark Mode of inheritance for gene: CACNB4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Brain Channelopathies v0.3 CACNB4 Zornitza Stark Marked gene: CACNB4 as ready
Brain Channelopathies v0.3 CACNB4 Zornitza Stark Gene: cacnb4 has been classified as Amber List (Moderate Evidence).
Brain Channelopathies v0.3 CACNB4 Zornitza Stark Phenotypes for gene: CACNB4 were changed from to Episodic ataxia, type 5, MIM#613855
Brain Channelopathies v0.2 CACNB4 Zornitza Stark Publications for gene: CACNB4 were set to
Brain Channelopathies v0.1 CACNB4 Zornitza Stark Classified gene: CACNB4 as Amber List (moderate evidence)
Brain Channelopathies v0.1 CACNB4 Zornitza Stark Gene: cacnb4 has been classified as Amber List (Moderate Evidence).
Brain Channelopathies v0.0 CACNB4 Zornitza Stark reviewed gene: CACNB4: Rating: AMBER; Mode of pathogenicity: None; Publications: 10762541, 9628818, 27003325; Phenotypes: Episodic ataxia, type 5, MIM#613855; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Brain Channelopathies v0.0 CACNB4 Zornitza Stark gene: CACNB4 was added
gene: CACNB4 was added to Channelopathy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: CACNB4 was set to Unknown