KCNT1

Gene

potassium sodium-activated channel subfamily T member 1

HGNCHGNC:18865 EnsemblENSG00000107147 NCBI Gene57582

Locus: gene with protein productLocation: 9q34.3

Also known as

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

Also known asKCa4.1 · KIAA1422 · SLACK · Slo2.2

View full nomenclature history (7)

Alias symbolsKCa4.1, KIAA1422, SLACK, Slo2.2

Previous namespotassium channel, subfamily T, member 1, potassium channel, sodium activated subfamily T, member 1

Alias namesSequence like a calcium-activated K+ channel

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.

Autosomal dominant nocturnal frontal lobe epilepsy

Genetic Diseases, Inborn

Epilepsy

Sleep-related hypermotor epilepsy

Familial sleep-related hypermotor epilepsy

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 sodium-activated channel subfamily T

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.