Back to discover

KCNJ5

Gene

potassium inwardly rectifying channel subfamily J member 5

HGNCHGNC:6266EnsemblENSG00000120457NCBI Gene3762
Locus: gene with protein productLocation: 11q24.3

Also known as

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

Also known asKir3.4 · CIR · KATP1 · GIRK4 · LQT13
View full nomenclature history (7)
Alias symbolsKir3.4, CIR, KATP1, GIRK4, LQT13
Previous namespotassium inwardly-rectifying channel, subfamily J, member 5
Alias namesG protein-activated inward rectifier potassium channel 4

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.

Atrial Fibrillation
Adrenocortical Adenoma
Arrhythmias, Cardiac
Atrial Flutter

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.

Potassium inwardly rectifying channel subfamily J

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.