CCDC175

Gene

coiled-coil domain containing 175

HGNCHGNC:19847 EnsemblENSG00000151838 NCBI Gene729665

Locus: gene with protein productLocation: 14q23.1

Also known as

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

Also known asC14orf38

View full nomenclature history (2)

Previous symbolsC14orf38

Previous nameschromosome 14 open reading frame 38

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

Sleep Initiation and Maintenance Disorders

Raynaud's Disease

Thyroiditis, Autoimmune

Major depressive disorder

Smoking initiation

Schizophrenia

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.