Predicted to enable transmembrane transporter activity. Predicted to be involved in transmembrane transport. Predicted to be active in membrane. Is expressed in intestine and pharyngeal neurons. Human ortholog(s) of this gene implicated in hereditary folate malabsorption. Orthologous to several human genes including SLC46A1 (solute carrier family 46 member 1).
WB Description
Predicted to enable transmembrane transporter activity. Predicted to be involved in transmembrane transport. Predicted to be located in membrane. Expressed in intestine and pharyngeal neurons. Human ortholog(s) of this gene implicated in hereditary folate malabsorption. Is an ortholog of human SLC46A1 (solute carrier family 46 member 1).