FOXI1
Sign in to saveAlso known as HFH3, FKH10, FKHL10, FREAC-6, FREAC6, HFH-3, forkhead box I1
Forkhead box I1 is a protein that in humans is encoded by the FOXI1 gene.
In the Vinony graph
Vinony's link graph records 893 inbound references to FOXI1, and connects out to PubMed, human chromosome 5 and Ensembl genome database project.
It is catalogued under topics including Forkhead transcription factors and Genes on human chromosome 5.
Vinony links it to 5 Wikipedia language editions.
Gene data
FOXI1- Name
- forkhead box I1
- Type
- protein-coding
- Position
- 170,105,893–170,109,734 (+)
- Aliases
- FKH10, FKHL10, FREAC-6, FREAC6, HFH-3, HFH3
- Ensembl
- ENSG00000168269
- RefSeq RNA
- NM_012188.5, NM_144769.4, XR_008487100.1, XR_941092.2
- RefSeq protein
- NP_036320.2, NP_658982.1
This gene belongs to the forkhead family of transcription factors, which is characterized by a distinct forkhead domain. This gene may play an important role in the development of the cochlea and vestibulum, as well as in embryogenesis. The encoded protein has been found to be required for the transcription of four subunits of a proton pump found in the inner ear, the kidney, and the epididymis. Mutations in this gene have been associated with deafness, autosomal recessive 4. [provided by RefSeq, Jan 2017].
Gene Ontology
Biological process
Molecular function
via MyGene.info
Gene · Ensembl
forkhead box I1
- Symbol
- FOXI1
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 5:170,105,893-170,109,734
- Strand
- Forward (+)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 7 more facts
- HomoloGene ID
- 8140
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/2299
- genomic end
- 170109734
- genomic start
- 169532901
- chromosome
- human chromosome 5
- cytogenetic location
- 5q35.1
Sources (3)
via Wikidata · CC0
~1 min read
Encyclopedic overview
5 sectionsContents
- Clinical significance
- See also
- References
- Further reading
- External links
Forkhead box I1 is a protein that in humans is encoded by the FOXI1 gene.
This gene belongs to the forkhead family of transcription factors which is characterized by a distinct forkhead domain. The specific function of this gene has not yet been determined; however, it is possible that this gene plays an important role in the development of the cochlea and vestibulum, as well as embryogenesis. Two transcript variants encoding different isoforms have been found for this gene.
Excerpted from Wikipedia’s “FOXI1” article, available under the CC BY-SA 4.0 licence.