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KCNA1
potassium voltage-gated channel subfamily A member 1
gene with protein product
OMIM: 176260
5 заболеваний
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Герминативная мутация (причина)
5
Isolated autosomal dominant hypomagnesemia, Glaudemans type
ORPHA:199326
→
Early infantile developmental and epileptic encephalopathy
ORPHA:1934
→
Hereditary continuous muscle fiber activity
ORPHA:972
→
Episodic ataxia type 1
ORPHA:37612
→
Paroxysmal kinesigenic dyskinesia
ORPHA:98809
→
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Редкие заболевания
KCNA1
🧬
KCNA1
potassium voltage-gated channel subfamily A member 1
gene with protein product
OMIM: 176260
5 заболеваний
GeneCards ↗
Open Targets ↗
NCBI Gene ↗
OMIM ↗
Ассоциированные заболевания
Герминативная мутация (причина)
5
Isolated autosomal dominant hypomagnesemia, Glaudemans type
ORPHA:199326
→
Early infantile developmental and epileptic encephalopathy
ORPHA:1934
→
Hereditary continuous muscle fiber activity
ORPHA:972
→
Episodic ataxia type 1
ORPHA:37612
→
Paroxysmal kinesigenic dyskinesia
ORPHA:98809
→