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KCND3 - potassium voltage-gated channel subfamily D member 3
- Synonym(s) : KSHIVB, Kv4.3
- Previous symbols and names : SCA19, SCA22, potassium voltage-gated channel, Shal-related subfamily, member 3, spinocerebellar ataxia 19, spinocerebellar ataxia 22
- Type : gene with protein product
- Chromosomal location : 1p13.2
- OMIM: 605411
- HGNC: 6239
- UniProtKB: Q9UK17
- Genatlas: KCND3
- GenCC: KCND3
- Ensembl: ENSG00000171385
- IUPHAR-DB: 554
- Reactome: Q9UK17
- LOVD: KCND3
Diseases list
- Disease-causing germline mutation(s) in Spinocerebellar ataxia type 19/22
ORPHA:98772 
- Candidate gene tested in Brugada syndrome
ORPHA:130
: AssessedAdditional information
Patient-centred resources for this gene
Research activities on this gene
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