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CLCNKB - chloride voltage-gated channel Kb
- Synonym(s) : hClC-Kb
- Previous symbols and names : Chloride channel Kb, chloride channel, voltage-sensitive Kb
- Type : gene with protein product
- Chromosomal location : 1p36.13
- OMIM: 602023
- HGNC: 2027
- UniProtKB: P51801
- Genatlas: CLCNKB
- Ensembl: ENSG00000184908
- IUPHAR-DB: -
- Reactome: P51801
- LOVD: CLCNKB
Diseases list
- Disease-causing germline mutation(s) in Classic Bartter syndrome
ORPHA:93605 
- Disease-causing germline mutation(s) (loss of function) in Gitelman syndrome
ORPHA:358 - Disease-causing germline mutation(s) (loss of function) in Infantile Bartter syndrome with sensorineural deafness
ORPHA:89938
: AssessedGene included in a panel of genes performed as part of a diagnostic test
Additional information
Health care resources for this gene
Research activities on this gene
Specialised Social Services
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