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HTR1D

Gene

5-hydroxytryptamine receptor 1D

HGNCHGNC:5289EnsemblENSG00000179546NCBI Gene3352
Locus: gene with protein productLocation: 1p36.12

Also known as

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

Also known asHTRL · RDC4 · HT1DA · 5-HT1D
View full nomenclature history (6)
Previous symbolsHTRL
Alias symbolsRDC4, HT1DA, 5-HT1D
Previous names5-hydroxytryptamine (serotonin) receptor 1D, 5-hydroxytryptamine (serotonin) receptor 1D, G protein-coupled

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.

Migraine Disorders
Schizophrenia
Epilepsies, Myoclonic
Major depressive disorder
Obesity disorder
Epilepsy

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.

5-hydroxytryptamine receptors, G protein-coupled

Provenance

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