FOXP1

Gene

forkhead box P1

HGNCHGNC:3823 EnsemblENSG00000114861 NCBI Gene27086

Locus: gene with protein productLocation: 3p13

Also known as

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

Also known asQRF1 · 12CC4 · HSPC215 · hFKH1B

View full nomenclature history (7)

Alias symbolsQRF1, 12CC4, HSPC215, hFKH1B

Alias namesfork head-related protein like B, glutamine-rich factor 1, PAX5/FOXP1 fusion protein

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.

Genetic Diseases, Inborn

Attention Deficit Disorder with Hyperactivity

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 boxesMicroRNA protein coding host genes

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2025-04-24.

Open TargetsGene–disease associations from the Open Targets Platform.