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Brain Channelopathies v0.46 KCNA1 Zornitza Stark Marked gene: KCNA1 as ready
Brain Channelopathies v0.46 KCNA1 Zornitza Stark Gene: kcna1 has been classified as Green List (High Evidence).
Brain Channelopathies v0.46 KCNA1 Zornitza Stark Phenotypes for gene: KCNA1 were changed from Episodic ataxia/myokymia syndrome, MIM# 160120 to Episodic ataxia/myokymia syndrome, MIM# 160120
Brain Channelopathies v0.45 KCNA1 Zornitza Stark Phenotypes for gene: KCNA1 were changed from to Episodic ataxia/myokymia syndrome, MIM# 160120
Brain Channelopathies v0.44 KCNA1 Zornitza Stark Publications for gene: KCNA1 were set to 11026449
Brain Channelopathies v0.44 KCNA1 Zornitza Stark Publications for gene: KCNA1 were set to
Brain Channelopathies v0.43 KCNA1 Zornitza Stark Mode of pathogenicity for gene: KCNA1 was changed from to Other
Brain Channelopathies v0.42 KCNA1 Zornitza Stark Mode of inheritance for gene: KCNA1 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Brain Channelopathies v0.0 KCNA1 Zornitza Stark gene: KCNA1 was added
gene: KCNA1 was added to Channelopathy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: KCNA1 was set to Unknown