Predicted to enable salt transmembrane transporter activity. Predicted to be involved in inorganic anion transmembrane transport and organic anion transport. Predicted to be located in membrane. Expressed in
pm3;
pm4;
pm5;
pm6; and
pm7. Human ortholog(s) of this gene implicated in autosomal recessive nonsyndromic deafness 61 and spermatogenic failure 3. Is an ortholog of several human genes including SLC26A6 (solute carrier family 26 member 6); SLC26A7 (solute carrier family 26 member 7); and SLC26A9 (solute carrier family 26 member 9).