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CLRN1

Gene

clarin 1

HGNCHGNC:12605EnsemblENSG00000163646NCBI Gene7401
Locus: gene with protein productLocation: 3q25.1

Also known as

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

Also known asUSH3 · USH3A · RP61
View full nomenclature history (4)
Previous symbolsUSH3, USH3A, RP61
Previous namesUsher syndrome 3A

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.

Retinitis Pigmentosa
Neuronal Ceroid-Lipofuscinoses
Hearing Loss
Eye Diseases

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 2023-03-15.
Open TargetsGene–disease associations from the Open Targets Platform.