Back to discover

OR2L13

Gene

olfactory receptor family 2 subfamily L member 13

HGNCHGNC:19578EnsemblENSG00000196071NCBI Gene284521
Locus: gene with protein productLocation: 1q44

Also known as

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

Also known asOR2L14
View full nomenclature history (2)
Previous symbolsOR2L14
Previous namesolfactory receptor, family 2, subfamily L, member 13

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
Keratitis
Autosomal dominant macrothrombocytopenia

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.

Olfactory receptors, family 2

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.