Automated description from the Alliance of Genome Resources (Release 4.0)
Predicted to have ABC-type xenobiotic transporter activity and protein domain specific binding activity. Predicted to be involved in several processes, including carboxylic acid transport; cellular chloride ion homeostasis; and drug export. 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).