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CCDC136

Gene

coiled-coil domain containing 136

HGNCHGNC:22225EnsemblENSG00000128596NCBI Gene64753
Locus: gene with protein productLocation: 7q32.1

Also known as

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

Also known asKIAA1793 · NAG6 · DKFZP434G156
View full nomenclature history (3)
Alias symbolsKIAA1793, NAG6, DKFZP434G156

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.

Neurodegenerative Diseases
Atrial Fibrillation
Heart Failure
Arrhythmias, Cardiac
Cardiomyopathy, Dilated
Cardiomyopathy, Hypertrophic
Paroxysmal tachycardia
Cardiomyopathies
Heart Failure, Systolic

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.

Provenance

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