Gene: FOXI1

Alternate names for this Gene: FKH10|FKHL10|FREAC-6|FREAC6|HFH-3|HFH3

Gene 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.

Gene is located in Chromosome: 5

Location in Chromosome : 5q35.1

Description of this Gene: forkhead box I1

Type of Gene: protein-coding

rs10057744 in FOXI1 gene and Leukemia, Myelocytic, Acute PMID 27903959 2017 Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.