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FOXP3

Gene

forkhead box P3

HGNCHGNC:6106EnsemblENSG00000049768NCBI Gene50943
Locus: gene with protein productLocation: Xp11.23

Also known as

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

Also known asIPEX · JM2 · XPID · AIID · PIDX · DIETER · SCURFIN
View full nomenclature history (8)
Previous symbolsIPEX
Alias symbolsJM2, XPID, AIID, PIDX, DIETER, SCURFIN
Previous namesimmune dysregulation, polyendocrinopathy, enteropathy, X-linked

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.

Diabetes Mellitus, Type 1
Hydrops fetalis
Neurodegenerative Diseases
Neurodevelopmental Disorders
Genetic Diseases, Inborn
Lupus Erythematosus, Systemic

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.

Forkhead boxes

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2025-10-10.
Open TargetsGene–disease associations from the Open Targets Platform.