Automated description from the Alliance of Genome Resources (Release 3.0)
Predicted to have ATPase-coupled transmembrane transporter activity; protein domain specific binding activity; and xenobiotic transmembrane transporter activity. Predicted to be involved in several processes, including carboxylic acid transport; cellular chloride ion homeostasis; and xenobiotic detoxification by transmembrane export across the plasma membrane. Localizes to apical plasma membrane; integral component of plasma membrane; and intercellular canaliculus. Human ortholog(s) of this gene implicated in several diseases, including bile duct disease (multiple); bilirubin metabolic disorder (multiple); drug-induced hepatitis; leukemia (multiple); and non-alcoholic fatty liver disease. Orthologous to human ABCC2 (ATP binding cassette subfamily C member 2).