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FOXP2

Gene

forkhead box P2

HGNCHGNC:13875EnsemblENSG00000128573NCBI Gene93986
Locus: gene with protein productLocation: 7q31.1

Also known as

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

Also known asTNRC10 · SPCH1 · CAGH44
View full nomenclature history (7)
Previous symbolsTNRC10, SPCH1
Alias symbolsCAGH44
Alias namesspeech and language disorder 1, trinucleotide repeat containing 10, forkhead/winged-helix transcription factor, CAG repeat protein 44

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
Osteoarthritis
Risk-taking behaviour
Substance-Related Disorders
Sleep Initiation and Maintenance Disorders
Stress Disorders, Post-Traumatic

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 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.