FoxI1 Polyclonal Antibody, 100ul DNA/RNA Isolation & Purification The protein encoded by this

The protein encoded by this gene is a member of the interleukin 1 receptor family and is similar to the interleukin 1 accessory proteins

Mutations in this gene result in epimerase-deficiency galactosemia| also referred to as galactosemia type 3| a disease characterized by liver damage| early-onset cataracts| deafness and mental retardation| with symptoms ranging from mild ('peripheral' form) to severe ('generalized' form)

enhancing selectively low-frequency neurotransmission

This gene encodes a growth factor receptor-binding protein that interacts with insulin receptors and insulin-like growth-factor receptors

which encode a phylogenetically conserved family of transcription factors that regulate a variety of developmental processes

FoxI1 Polyclonal Antibody, 100ul DNA/RNA Isolation & Purification The protein encoded by thisFOXI1 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