T10F2.2 is orthologous to the human gene SOLUTE CARRIER FAMILY 25 (MITOCHONDRIAL CARRIER; ORNITHINE TRANSPORTER) MEMBER 15 (SLC25A15; OMIM:603861), which when mutated leads to disease.
Predicted to enable L-ornithine transmembrane transporter activity. Predicted to be involved in mitochondrial L-ornithine transmembrane transport. Predicted to be located in mitochondrion. Expressed in tail. Human ortholog(s) of this gene implicated in citrullinemia and ornithine translocase deficiency. Is an ortholog of human SLC25A15 (solute carrier family 25 member 15) and SLC25A2 (solute carrier family 25 member 2).