Automated description from the Alliance of Genome Resources
Predicted to have 4-hydroxybutyrate receptor activity and riboflavin transmembrane transporter activity. Predicted to be involved in riboflavin transport. Predicted to localize to the integral component of plasma membrane. Human ortholog(s) of this gene implicated in Brown-Vialetto-Van Laere syndrome and ariboflavinosis. Orthologous to several human genes including SLC52A2 (solute carrier family 52 member 2).