FOXI1 Back

forkhead box I1

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NCBI Description of FOXI1

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.

Community Annotation of FOXI1 Add / Edit FOXI1: Annotations

No community annotations yet for FOXI1.
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Figure notes

• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


FOXI1 is highly significantly mutated in
FOXI1 is significantly mutated in
FOXI1 is near significance in

Click on a tumor type to see its full list of significant genes.

Data details

Mutation list for FOXI1