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KCNE5 - potassium voltage-gated channel subfamily E regulatory subunit 5
- Synonym(s) :
- Previous symbols and names : KCNE1L, potassium channel, voltage gated subfamily E regulatory beta subunit 5, potassium voltage-gated channel, Isk-related family, member 1-like
- Type : gene with protein product
- Chromosomal location : Xq23
- OMIM: 300328
- HGNC: 6241
- UniProtKB: Q9UJ90
- Genatlas: KCNE1L
- GenCC: KCNE1L
- Ensembl: ENSG00000176076
- IUPHAR-DB: -
- Reactome: Q9UJ90
- LOVD: KCNE5
Diseases list
- Role in the phenotype of Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome
ORPHA:86818 
- Candidate gene tested in Brugada syndrome
ORPHA:130
: AssessedAdditional information
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