S26A5 Polyclonal Antibody, 100ul[BT-AP14007] Buffers & Solutions This gene has a mouse

This gene has a mouse ortholog

Alternative splicing of downstream exons is also observed

|PTM:Citrullination at Arg-4 by PADI4 impairs methylation

Mutations in this gene have been found to cause fish-eye disease as well as LCAT deficiency

and mutations in this gene result in type II diabetes mellitus

S26A5 Polyclonal Antibody, 100ul[BT-AP14007] Buffers & Solutions This gene has a mouseThis gene encodes a member of the SLC26A SulP transporter family. The protein functions as a molecular motor in motile outer hair cells (OHCs) of the cochlea, inducing changes in cell length that act to amplify sound levels. The transmembrane protein is an incomplete anion transporter, and does not allow anions to cross the cell membrane but instead undergoes a conformational change in response to changes in intracellular Cl levels that results in a