Automated description from the Alliance of Genome Resources
Predicted to have ion transmembrane transporter activity and protein dimerization activity. Involved in fluid transport and ion homeostasis. Predicted to localize to the integral component of membrane and plasma membrane. Used to study congenital hereditary endothelial dystrophy of cornea. Human ortholog(s) of this gene implicated in Fuchs' endothelial dystrophy and congenital hereditary endothelial dystrophy of cornea. Is expressed in metanephros and vomeronasal organ. Orthologous to human SLC4A11 (solute carrier family 4 member 11).