Automated description from the Alliance of Genome Resources (Release 7.0.0)
Predicted to enable L-aspartate transmembrane transporter activity; L-glutamate transmembrane transporter activity; and amino acid:proton symporter activity. Predicted to be involved in amino acid transmembrane transport; malate-aspartate shuttle; and regulation of insulin secretion. Located in mitochondrion. Is expressed in alimentary system; eye; liver; and nervous system. Human ortholog(s) of this gene implicated in developmental and epileptic encephalopathy 3. Orthologous to human SLC25A22 (solute carrier family 25 member 22).