Back to discover

OTOGL

Gene

otogelin like

HGNCHGNC:26901EnsemblENSG00000165899NCBI Gene283310
Locus: gene with protein productLocation: 12q21.31

Also known as

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

Also known asC12orf64 · FLJ90579
View full nomenclature history (4)
Previous symbolsC12orf64
Alias symbolsFLJ90579
Previous nameschromosome 12 open reading frame 64, otogelin-like

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
Vestibular Diseases
Nonsyndromic genetic hearing loss
Non-syndromic genetic deafness
Genetic Diseases, Inborn

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