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CLCNKB

Gene

chloride voltage-gated channel Kb

HGNCHGNC:2027EnsemblENSG00000184908NCBI Gene1188
Locus: gene with protein productLocation: 1p36.13

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known ashClC-Kb · CLCKB · ClC-K2 · ClC-Kb
View full nomenclature history (7)
Alias symbolshClC-Kb, CLCKB, ClC-K2, ClC-Kb
Previous nameschloride channel Kb, chloride channel, voltage-sensitive Kb
Alias namesChloride channel protein ClC-Kb

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Bartter Syndrome
Gitelman Syndrome
Prostate carcinoma

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

CLC chloride channel and transporter family

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-25.
Open TargetsGene–disease associations from the Open Targets Platform.