Automated description from the Alliance of Genome Resources
Predicted to have PDZ domain binding activity; protein homodimerization activity; and transmembrane transporter activity. Involved in bone remodeling. Localizes to the basolateral plasma membrane and vesicle. Used to study hereditary hypophosphatemic rickets with hypercalciuria. Human ortholog(s) of this gene implicated in several diseases, including Fanconi syndrome; chronic kidney disease; hereditary hypophosphatemic rickets with hypercalciuria; hypophosphatemic nephrolithiasis/osteoporosis 1; and nephrolithiasis. Orthologous to human SLC34A1 (solute carrier family 34 member 1).