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KCNQ3 - potassium voltage-gated channel subfamily Q member 3
- Synonym(s) : Kv7.3
- Previous symbols and names : EBN2, potassium channel, voltage gated KQT-like subfamily Q, member 3, potassium voltage-gated channel, KQT-like subfamily, member 3
- Type : gene with protein product
- Chromosomal location : 8q24.22
- OMIM: 602232
- HGNC: 6297
- UniProtKB: O43525
- Genatlas: KCNQ3
- GenCC: KCNQ3
- Ensembl: ENSG00000184156
- IUPHAR-DB: 562
- Reactome: O43525
- LOVD: KCNQ3
Diseases list
- Disease-causing germline mutation(s) in Benign familial infantile epilepsy
ORPHA:306 
- Disease-causing germline mutation(s) in Benign familial neonatal epilepsy
ORPHA:1949 - Major susceptibility factor in Juvenile myoclonic epilepsy
ORPHA:307
: AssessedAdditional information
Patient-centred resources for this gene
Research activities on this gene
Specialised Social Services
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