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Gene · 27086

FOXP1: forkhead box P1

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

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ConductScience Library. FOXP1: forkhead box P1. Genes, record 27086. Release gene-search-2026-11-11-0.2.0, 11 Nov 2026. https://conductscience.org/library/genes/27086

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Gene

Symbol
FOXP1
HGNC
Name
forkhead box P1
HGNC
NCBI Gene ID
27086
NCBI Gene
HGNC ID
HGNC:3823
HGNC
Ensembl
ENSG00000114861
NCBI Gene
Aliases
12CC4, HSPC215, MFH, QRF1, hFKH1B
NCBI Gene
Type
protein-coding
NCBI Gene

Proteins1

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

UniProt entryProteinLengthStructuresGene stated in
Q9H334Forkhead box protein P16771Ensembl, GeneID, HGNC

Source UniProt

Patents67

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

PublicationPublishedSEQ ID NOProteinSource
EP 4698657 A22026-02-25377Q9H334Espacenet
JP 2026004568 A2026-01-1446566Q9H334Espacenet
JP 2026004568 A2026-01-1446570Q9H334Espacenet
JP 2026004568 A2026-01-1446575Q9H334Espacenet
EP 4650780 A22025-11-195224Q9H334Espacenet
EP 4641201 A22025-10-294807Q9H334Espacenet
JP 2025147176 A2025-10-0615014Q9H334Espacenet
JP 2025517969 A2025-06-124807Q9H334Espacenet
JP 2025517970 A2025-06-125224Q9H334Espacenet
JP 2025028160 A2025-02-2815014Q9H334Espacenet

1 to 10 of 67

See all 67 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 grants2,986

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

GrantTitleFOXP1 papersNewest fiscal year
P30CA008748Cancer Center Support Grant322025
P30CA016672Cancer Center Support Grant242025
R01MH101221Rare Mutations and Autism Spectrum Disorders132025
ZIASC000550Lymphoma Disease Discovery and Definition102025
P30CA006973Regional Oncology Research Center72025
P30CA016058Cancer Center Support Grant72025
P30CA060553The Robert H. Lurie Comprehensive Cancer Center72025
P30CA010815Consolidated Basic Cancer Research Program62025
P30CA021765Cancer Center Support Grant (CCSG)62025
P50CA092629SPORE in Prostate Cancer62025

1 to 10 of 2,986Source NIH's project files

See all 2,986 nih grants

Papers3,898

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
FOXP1 Knockdown Reprograms Th9 CAR-T Cells to Overcome Antigen Escape.Adv Sci (Weinh)202642750117PubTator, text miningPubMed
Prenatal exposure to the plasticizer DEHP increases the likelihood of early-life autism and ADHD symptoms through epigenetic programming.Med202642727573PubTator, text miningPubMed
Severe Headbanging Responsive to Levodopa in a Child With FOXP1 Syndrome.Am J Med Genet A202642711896PubTator, text miningPubMed
STK31 enhances gallbladder cancer development by modulating DNA replication machinery.J Biol Chem202642710668PubTator, text miningPubMed
Peripheral γδ T-cell remodeling in psoriasis is associated with effector-biased transcriptional organization and reduced representation of a circulating CSMD1-marked state.Front Immunol202642694189PubTator, text miningPubMed
Facebook as a Lifeboat: An Interview Study Exploring the Role of Facebook in Supporting Parents of Children with Rare Diseases.J Health Commun202642687858PubTator, text miningPubMed
Autism mutations rewire protein interaction networks to drive neurodevelopmental pathology.Science202642658940PubTator, text miningPubMed
Photodynamic priming enhances anti-PD1 therapy responses in patient-derived pancreatic cancer organoid immune cocultures.Front Immunol202642643393PubTator, text miningPubMed
LncRNA HOTAIR/miR-9-5p/FOXP1 axis modulates cerebral ischemia-reperfusion injury via NLRP3 inflammasome activation.IBRO Neurosci Rep202642621072PubTator, 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

1 to 10 of 3,898

See all 3,898 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/v1/27086

GET https://conductscience.org/api/genes/v1/27086/patents?page=2