FOXI1 forkhead box I1 [ Homo sapiens (human) ]
Source: NCBI Gene (ID 2299)
Source: NCBI Gene (ID 2299)
Symbol: FOXI1
Full name: forkhead box I1
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: FKH10; FKHL10; FREAC-6; FREAC6; HFH-3; HFH3
Summary: 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]
Expression: Biased expression in kidney (RPKM 10.3), salivary gland (RPKM 2.7) and 1 other tissue
Orthologs: mouse
Gene size: 3841bp
Exon count: 3