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FOXI1, forkhead box I1

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FOXI1, forkhead box I1

  • 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 Synonyms (FKH10, FKHL10, FREAC-6, FREAC6, HFH-3, HFH3, forkhead box protein I1, HNF-3/fork-head homolog-3, forkhead-like 10, forkhead-related activator 6, forkhead-related protein FKHL10, forkhead-related transcription factor 6, hepatocyte nuclear factor 3 forkhead homolog 3,)
  • NCBI Gene ID: 2299
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q12951
    UNIPROT ID#>>E0XEN6
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

forkhead box I1 interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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