S22A2 Polyclonal Antibody, 50ul Culture Plate Inserts Mutations in this gene are

Mutations in this gene are associated with autosomal recessive deafness type 22 (DFNB22)

Two transcripts

It is an accessory chain essential for the active interleukin 10 receptor complex

The encoded preproprotein is proteolytically processed to generate the mature enzyme

Involved in signal transduction through the Wnt pathway

S22A2 Polyclonal Antibody, 50ul Culture Plate Inserts Mutations in this gene arePolyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. This gene is one of three similar cation transporter genes located in a cluster on chromosome 6. The encoded protein contains twelve putative transmembrane domains and is a plasma integral membrane protein. It is found primarily in the