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KCNA1

potassium voltage-gated channel subfamily A member 1

gene with protein productOMIM: 1762605 заболеваний
GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Герминативная мутация (причина)5
Isolated autosomal dominant hypomagnesemia, Glaudemans typeORPHA:199326
→
Early infantile developmental and epileptic encephalopathyORPHA:1934
→
Hereditary continuous muscle fiber activityORPHA:972
→
Episodic ataxia type 1ORPHA:37612
→
Paroxysmal kinesigenic dyskinesiaORPHA:98809
→
Данные: Orphadata (CC-BY-4.0)