| Entrez gene ID | | 2299 |
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| Official gene symbol | | FOXI1 |
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| Full name | | forkhead box I1 |
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| Aliases | | ,FKH10,FKHL10,FREAC6,HFH3,MGC34197, |
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| Gene summary | | 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. Mutations in this gene may be associated with the common cavity phenotype. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq] |
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| Location | | Chromosome: 5 Locus: 5q34 |
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| Gene position | | 169532917 - 169536729 Map Viewer |
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| Gene orientation | | plus |
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| Gene size | | 3813 bp |
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| Gene sequence |
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| OMIM ID | | 601093 |
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