Slc4a11 - solute carrier family 4 member 11

Predicted to enable ion transmembrane transporter activity; protein dimerization activity; and water transmembrane transporter activity. Predicted to be involved in several processes, including anion transport; cation transport; and cellular hypotonic response. Located in basolateral plasma membrane and vesicle membrane. Human ortholog(s) of this gene implicated in Fuchs' endothelial dystrophy; congenital hereditary endothelial dystrophy of cornea; and corneal dystrophy-perceptive deafness syndrome. Orthologous to human SLC4A11 (solute carrier family 4 member 11). [provided by Alliance of Genome Resources, Apr 2022]