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GPR42

Gene

G protein-coupled receptor 42

HGNCHGNC:4500EnsemblENSG00000126251NCBI Gene2866
Locus: gene with protein productLocation: 19q13.12

Also known as

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

Also known asGPR42P · GPR41L · FFAR3L
View full nomenclature history (5)
Previous symbolsGPR42P
Alias symbolsGPR41L, FFAR3L
Previous namesG protein-coupled receptor 42 pseudogene, G protein-coupled receptor 42 (gene/pseudogene)

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.

hyperinsulinism due to INSR deficiency

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.

G protein-coupled receptors, Class A orphans

Provenance

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