Gene · 2290
FOXG1: forkhead box G1
12 sourcesgene-search-2026-11-11-0.2.0
Cite this record
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
On this page
Gene
Proteins1
Reviewed human proteins whose Swiss-Prot entry states the gene.
| UniProt entry | Protein | Length | Structures | Gene stated in |
|---|---|---|---|---|
| P55316 | Forkhead box protein G1 | 489 | 1 | Ensembl, GeneID, HGNC |
Source UniProt
Patents37
Patents whose sequence listing contains this protein's exact sequence. A patent can list a sequence without claiming it.
| Publication | Published | SEQ ID NO | Protein | Source |
|---|---|---|---|---|
| JP 2026004568 A | 2026-01-14 | 46540 | P55316 | Espacenet |
| JP 2026004568 A | 2026-01-14 | 46541 | P55316 | Espacenet |
| EP 4641201 A2 | 2025-10-29 | 6154 | P55316 | Espacenet |
| JP 2025147176 A | 2025-10-06 | 14993 | P55316 | Espacenet |
| JP 2025517969 A | 2025-06-12 | 6154 | P55316 | Espacenet |
| JP 2025032204 A | 2025-03-11 | 28554 | P55316 | Espacenet |
| JP 2025028160 A | 2025-02-28 | 14993 | P55316 | Espacenet |
| KR 1020250010750 A | 2025-01-21 | 14993 | P55316 | Espacenet |
| EP 4461818 A2 | 2024-11-13 | 28554 | P55316 | Espacenet |
| JP 2024109657 A | 2024-08-14 | 14832 | P55316 | Espacenet |
1 to 10 of 37
See all 37 patentsDrugs0
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.
| Grant | Title | FOXG1 papers | Newest fiscal year |
|---|---|---|---|
| P30CA008748 | Cancer Center Support Grant | 24 | 2025 |
| ZIASC000550 | Lymphoma Disease Discovery and Definition | 10 | 2025 |
| R35NS116843 | Continuous Neurogenesis in the Mammalian Hippocampus | 8 | 2025 |
| ZIABC011070 | Hematopathology Diagnosis | 8 | 2025 |
| UL1TR001863 | Yale Clinical and Translational Science Award | 7 | 2025 |
| ZIEBC011241 | Hematopathology Fellowship | 7 | 2025 |
| P30CA016672 | Cancer Center Support Grant | 6 | 2025 |
| P50HD103537 | Overall: Eunice Kennedy Shriver Intellectual and Developmental Disabilities Research Center at Vanderbilt | 6 | 2025 |
| P50HD105351 | Boston Children's Hospital/HMS Intellectual and Developmental Disabilities Research Center | 6 | 2025 |
| R01NS058721 | ACC: Callosal Agenesis as a Window into Common Neurodevelopmental Disorders | 6 | 2025 |
1 to 10 of 2,369Source NIH's project files
See all 2,369 nih grantsPapers3,284
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| FOXG1 syndrome: genetic background revealed by trio WES in case of a critically ill neonate. | Ideggyogy Sz | 2026 | 42803093 | PubTator, text mining | PubMed |
| Transcriptome profiling of ocular surface ectoderm derived from embryonic stem cells, and identification of CACNG6 and AQP3 as its surface markers. | Int J Ophthalmol | 2026 | 42523845 | PubTator, text mining | PubMed |
| Nationwide Molecular Epidemiology of HIV-1 in Uruguay (2007-2021): Lineage Diversity, BF1 Recombinant Complexity and Epidemiological Patterns. | J Int AIDS Soc | 2026 | 42502233 | PubTator, text mining | PubMed |
| Analysis of 14q12 microdeletions reveals novel regulatory loci for the neurodevelopmental disorder-related gene FOXG1. | Nat Commun | 2026 | 42481467 | PubTator, text mining | PubMed |
| Clinical heterogeneity of primary cutaneous γδ T-cell lymphoma: a 20-year single-institution experience. | Blood Res | 2026 | 42477178 | PubTator, text mining | PubMed |
| Rapid and Robust Generation of Human Cortical Interneurons from Induced Neural Stem Cells. | Int J Mol Sci | 2026 | 42352918 | PubTator, text mining | PubMed |
| Integrated protocol for concurrent generation of microglial and neuronal cells in human cerebral organoids. | BMC Methods | 2026 | 42306776 | PubTator, text mining | PubMed |
| Genetic causes of the lissencephaly spectrum: insights from chromosomal microarray and clinical/whole-exome sequencing. | Croat Med J | 2026 | 42286901 | PubTator, text mining | PubMed |
| Evolutionary constraints impose multiple checkpoints that block mammalian sensory hair cell regeneration. | Front Cell Dev Biol | 2026 | 42245482 | PubTator, text mining | PubMed |
| Non-coding structural variants disrupt FOXG1 transcriptional regulation in early neurodevelopment. | Nat Commun | 2026 | 42236689 | PubTator, text mining | PubMed |
1 to 10 of 3,284
See all 3,284 papersSources 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