CLRN2

Gene

clarin 2

HGNCHGNC:33939 EnsemblENSG00000249581 NCBI Gene645104

Locus: gene with protein productLocation: 4p15.32

Also known as

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

Also known asDFNB117

View full nomenclature history (1)

Alias symbolsDFNB117

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

Presbycusis

Non-syndromic genetic deafness

Nonsyndromic genetic hearing loss

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.

Clarins

Provenance

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

Open TargetsGene–disease associations from the Open Targets Platform.