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NR4A2

Gene

nuclear receptor subfamily 4 group A member 2

HGNCHGNC:7981EnsemblENSG00000153234NCBI Gene4929
Locus: gene with protein productLocation: 2q24.1

Also known as

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

Also known asNURR1 · TINUR · NOT · RNR1 · HZF-3
View full nomenclature history (6)
Previous symbolsNURR1
Alias symbolsTINUR, NOT, RNR1, HZF-3
Previous namesnuclear receptor subfamily 4, group A, member 2

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.

Neurodevelopmental Disorders
Parkinson's Disease
Complex neurodevelopmental disorder
Genetic Diseases, Inborn
Drug Hypersensitivity

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.

Nuclear receptor subfamily 4 group A

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2024-01-15.
Open TargetsGene–disease associations from the Open Targets Platform.