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NR2F2

Gene

nuclear receptor subfamily 2 group F member 2

HGNCHGNC:7976EnsemblENSG00000185551NCBI Gene7026
Locus: gene with protein productLocation: 15q26.2

Also known as

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

Also known asARP1 · TFCOUP2 · SVP40 · COUP-TFII · COUPTFB · NF-E3 · COUPTF2
View full nomenclature history (9)
Previous symbolsARP1, TFCOUP2
Alias symbolsSVP40, COUP-TFII, COUPTFB, NF-E3, COUPTF2
Previous namesnuclear receptor subfamily 2, group F, member 2
Alias namesCOUP transcription factor II

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
Genetic Diseases, Inborn
Smoking initiation
Heart Defects, Congenital
Intelligence
Testicular Diseases

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.

MicroRNA protein coding host genesNuclear receptor subfamily 2 group F

Provenance

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