Back to discover

KCTD11

Gene

potassium channel tetramerization domain containing 11

HGNCHGNC:21302EnsemblENSG00000213859NCBI Gene147040
Locus: gene with protein productLocation: 17p13.1

Also known as

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

Also known asC17orf36 · REN · KCASH1
View full nomenclature history (5)
Previous symbolsC17orf36
Alias symbolsREN, KCASH1
Previous nameschromosome 17 open reading frame 36, potassium channel tetramerisation domain containing 11

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 secondary polycythemia
Neoplasms
Carcinoma, Hepatocellular
Carcinoma, Non-Small-Cell Lung
Lung Neoplasms

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.

KCTD family

Provenance

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