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Gene · 93986

FOXP2: forkhead box P2

12 sourcesgene-search-2026-11-11-0.2.0

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ConductScience Library. FOXP2: forkhead box P2. Genes, record 93986. Release gene-search-2026-11-11-0.2.0, 11 Nov 2026. https://conductscience.org/library/genes/93986

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Gene

Symbol
FOXP2
HGNC
Name
forkhead box P2
HGNC
NCBI Gene ID
93986
NCBI Gene
HGNC ID
HGNC:13875
HGNC
Ensembl
ENSG00000128573
NCBI Gene
Aliases
CAGH44, SPCH1, TNRC10
NCBI Gene
Type
protein-coding
NCBI Gene

Proteins1

Reviewed human proteins whose Swiss-Prot entry states the gene.

UniProt entryProteinLengthStructuresGene stated in
O15409Forkhead box protein P27152Ensembl, GeneID, HGNC

Source UniProt

Patents23

Patents whose sequence listing contains this protein's exact sequence. A patent can list a sequence without claiming it.

PublicationPublishedSEQ ID NOProteinSource
JP 2026004568 A2026-01-1446578O15409Espacenet
JP 2026004568 A2026-01-1446583O15409Espacenet
EP 4641201 A22025-10-292070O15409Espacenet
JP 2025517969 A2025-06-122070O15409Espacenet
US 12091439 B22024-09-1735O15409Espacenet
US 11446398 B22022-09-2032631O15409Espacenet
US 11446398 B22022-09-2032637O15409Espacenet
JP 2022524081 A2022-04-27135602O15409Espacenet
JP 2022524081 A2022-04-27135608O15409Espacenet
US 11274134 B22022-03-1535O15409Espacenet

1 to 10 of 23

See all 23 patents

Drugs0

Drugs a ChEMBL mechanism record says act on the gene's protein, through Open Targets.

None in this release.

Trials0

Trials of those drugs. A trial joins the gene only through a drug that acts on it.

None in this release.

NIH grants2,337

NIH grants whose papers are about the gene, through NIH's grant-paper links.

GrantTitleFOXP2 papersNewest fiscal year
P30CA008748Cancer Center Support Grant72025
P50HD027802Differential Diagnosis in Learning Disabilities72025
UL1TR001863Yale Clinical and Translational Science Award72025
P50HD052120Learning Disabilities Translational Science Collective: Building on the Florida LDRC52025
P51OD011132Emory National Primate Research Center52025
P30CA014195Cancer Center Support Grant (CCSG)42025
R01MH060379Functional and anatomical characterization of the striosomal system42025
T32GM008243UCLA Medical Genetics Training Program42025
DP1MH129954RNA-programmable cell-type targeting, editing, and therapy32025
P30CA015704Cancer Center Support Grant32025

1 to 10 of 2,337Source NIH's project files

See all 2,337 nih grants

Papers2,754

Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.

TitleJournalYearPMIDFound bySource
Autism genes converge on three functional programs organized by neuronal subclass, developmental timing, and cortical patterning.bioRxiv202642818021PubTator, text miningPubMed
Evaluating the pathogenic significance of unique chromosomal variants in craniosynostosis using patient-derived induced pluripotent stem cells and mouse modeling.Genet Med202642708327PubTator, text miningPubMed
Genetic Variation in ADHD-Related Risk Genes in an Indigenous Population of the Amazon.Am J Med Genet B Neuropsychiatr Genet202642581023PubTator, text miningPubMed
Molecular and cell type-specific determinants of inferior colliculus development and auditory function.bioRxiv202642539098PubTator, text miningPubMed
Parabrachial Ntsr1 neurons modulate food intake and anxiety through a projection to the ventromedial hypothalamus.Proc Natl Acad Sci U S A202642485394PubTator, text miningPubMed
Genomic landscape of rare variants in a Chinese autism cohort and discovery of novel risk genes.Mol Psychiatry202642463903PubTator, text miningPubMed
Genetic and molecular mechanisms of the FOXP2-CNTNAP2 pathway in Autism spectrum disorders and speech disorders.J Neural Transm (Vienna)202642455320PubTator, text miningPubMed
FOXP2+ Chief Cells and CXCL14+ Fibroblasts Drive Fibrotic Remodeling in Carotid Body Tumors.Int J Mol Sci202642450023PubTator, text miningPubMed
Metabolic Gating and the Evolution of Human Cognitive Plasticity: A Comparative Genomic Analysis.bioRxiv202642367946PubTator, text miningPubMed
FOXP Transcription Factors in Thyroid Cancer: From Molecular Expression to Clinical Significance.Biomedicines202642351648PubTator, text miningPubMed

1 to 10 of 2,754

See all 2,754 papers

Sources 12

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ChEMBL, through Open TargetsCC BY-SA 3.0
  • ClinicalTrials.govNo license stated
  • EMBL-EBI's patent proteinsNo added restrictions. Attribution expected
  • GenBank's patent filesNo restrictions from NCBI. Submitters may hold rights
  • HGNCCC0
  • NCBI GenePublic domain (US government)
  • NIH's project files and grant-paper linksPublic domain
  • Open TargetsCC0 1.0
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • ClinicalTrials.govnone stated
  • EMBL-EBI's patent proteinsEMBL-EBI's patent protein files from the EPO, JPO, KIPO and USPTO. EMBL-EBI: "EMBL-EBI itself places no additional restrictions on the use or redistribution of the data available via its Data Resources and Tools other than those provided by the original data owners" and "EMBL-EBI expects attribution (e.g. in publications, services or products) for the use of any of its Data Resources and Tools." Read on 11 Nov 2026 at https://www.ebi.ac.uk/about/terms-of-use
  • GenBank's patent filesGenBank's patent files. NCBI: "NCBI places no restrictions on the use or distribution of the GenBank data. However, some submitters may claim patent, copyright, or other intellectual property rights in all or a portion of the data they have submitted." Read on 11 Nov 2026 at https://www.ncbi.nlm.nih.gov/genbank/about/
  • HGNCCC0: https://www.genenames.org/about/license/
  • NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • NIH's project files and grant-paper linksPublic domain (NIH RePORTER)
  • Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this gene from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/genes/v1/93986

GET https://conductscience.org/api/genes/v1/93986/patents?page=2