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OR5T1

Gene

olfactory receptor family 5 subfamily T member 1

HGNCHGNC:14821EnsemblENSG00000181698NCBI Gene390155
Locus: gene with protein productLocation: 11q12.1

Also known as

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

Also known asOR5T1P
View full nomenclature history (2)
Previous symbolsOR5T1P
Previous namesolfactory receptor, family 5, subfamily T, member 1

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.

Female reproductive system disorder
Obesity disorder
Obesity due to melanocortin 4 receptor deficiency
Neuroblastoma

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 5

Provenance

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