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Gene · 2290

FOXG1: forkhead box G1

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

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ConductScience Library. FOXG1: forkhead box G1. Genes, record 2290. Release gene-search-2026-11-11-0.2.0, 11 Nov 2026. https://conductscience.org/library/genes/2290

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Gene

Symbol
FOXG1
HGNC
Name
forkhead box G1
HGNC
NCBI Gene ID
2290
NCBI Gene
HGNC ID
HGNC:3811
HGNC
Ensembl
ENSG00000176165
NCBI Gene
Aliases
BF1, BF2, FHKL3, FKH2, FKHL1, FKHL2, FKHL3, FKHL4, FOXG1A, FOXG1B, FOXG1C, HBF-1, HBF-2, HBF-3, HBF-G2, HBF2, HFK1, HFK2, HFK3, KHL2, QIN
NCBI Gene
Type
protein-coding
NCBI Gene

Proteins1

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

UniProt entryProteinLengthStructuresGene stated in
P55316Forkhead box protein G14891Ensembl, GeneID, HGNC

Source UniProt

Patents37

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

PublicationPublishedSEQ ID NOProteinSource
JP 2026004568 A2026-01-1446540P55316Espacenet
JP 2026004568 A2026-01-1446541P55316Espacenet
EP 4641201 A22025-10-296154P55316Espacenet
JP 2025147176 A2025-10-0614993P55316Espacenet
JP 2025517969 A2025-06-126154P55316Espacenet
JP 2025032204 A2025-03-1128554P55316Espacenet
JP 2025028160 A2025-02-2814993P55316Espacenet
KR 1020250010750 A2025-01-2114993P55316Espacenet
EP 4461818 A22024-11-1328554P55316Espacenet
JP 2024109657 A2024-08-1414832P55316Espacenet

1 to 10 of 37

See all 37 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 grants2,369

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

GrantTitleFOXG1 papersNewest fiscal year
P30CA008748Cancer Center Support Grant242025
ZIASC000550Lymphoma Disease Discovery and Definition102025
R35NS116843Continuous Neurogenesis in the Mammalian Hippocampus82025
ZIABC011070Hematopathology Diagnosis82025
UL1TR001863Yale Clinical and Translational Science Award72025
ZIEBC011241Hematopathology Fellowship72025
P30CA016672Cancer Center Support Grant62025
P50HD103537Overall: Eunice Kennedy Shriver Intellectual and Developmental Disabilities Research Center at Vanderbilt62025
P50HD105351Boston Children's Hospital/HMS Intellectual and Developmental Disabilities Research Center62025
R01NS058721ACC: Callosal Agenesis as a Window into Common Neurodevelopmental Disorders62025

1 to 10 of 2,369Source NIH's project files

See all 2,369 nih grants

Papers3,284

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
FOXG1 syndrome: genetic background revealed by trio WES in case of a critically ill neonate.Ideggyogy Sz202642803093PubTator, text miningPubMed
Transcriptome profiling of ocular surface ectoderm derived from embryonic stem cells, and identification of CACNG6 and AQP3 as its surface markers.Int J Ophthalmol202642523845PubTator, text miningPubMed
Nationwide Molecular Epidemiology of HIV-1 in Uruguay (2007-2021): Lineage Diversity, BF1 Recombinant Complexity and Epidemiological Patterns.J Int AIDS Soc202642502233PubTator, text miningPubMed
Analysis of 14q12 microdeletions reveals novel regulatory loci for the neurodevelopmental disorder-related gene FOXG1.Nat Commun202642481467PubTator, text miningPubMed
Clinical heterogeneity of primary cutaneous γδ T-cell lymphoma: a 20-year single-institution experience.Blood Res202642477178PubTator, text miningPubMed
Rapid and Robust Generation of Human Cortical Interneurons from Induced Neural Stem Cells.Int J Mol Sci202642352918PubTator, text miningPubMed
Integrated protocol for concurrent generation of microglial and neuronal cells in human cerebral organoids.BMC Methods202642306776PubTator, text miningPubMed
Genetic causes of the lissencephaly spectrum: insights from chromosomal microarray and clinical/whole-exome sequencing.Croat Med J202642286901PubTator, text miningPubMed
Evolutionary constraints impose multiple checkpoints that block mammalian sensory hair cell regeneration.Front Cell Dev Biol202642245482PubTator, text miningPubMed
Non-coding structural variants disrupt FOXG1 transcriptional regulation in early neurodevelopment.Nat Commun202642236689PubTator, text miningPubMed

1 to 10 of 3,284

See all 3,284 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/v1/2290

GET https://conductscience.org/api/genes/v1/2290/patents?page=2