CLIC5

Gene

CLIC family member 5

HGNCHGNC:13517 EnsemblENSG00000112782 NCBI Gene53405

Locus: gene with protein productLocation: 6p21.1

Also known as

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

Also known asDFNB102

View full nomenclature history (2)

Alias symbolsDFNB102

Previous nameschloride intracellular channel 5

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.

Hearing loss, autosomal recessive

Chronic venous hypertension

Diabetes Mellitus, Type 2

Severe Acute Respiratory Syndrome

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.

CLIC family

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2026-04-17.

Open TargetsGene–disease associations from the Open Targets Platform.