Automated description from the Alliance of Genome Resources
Predicted to have sphingolipid transporter activity. Involved in several processes, including lymph node development; lymphocyte homeostasis; and sphingosine-1-phosphate receptor signaling pathway. Predicted to localize to the integral component of membrane. Human ortholog(s) of this gene implicated in autosomal recessive nonsyndromic deafness. Is expressed in jaw bone; nervous system; and sensory organ. Orthologous to human SPNS2 (sphingolipid transporter 2).