Automated description from the Alliance of Genome Resources (Release 7.1.0)
Predicted to enable ABC-type transporter activity; bilirubin transmembrane transporter activity; and protein domain specific binding activity. Predicted to be involved in several processes, including carboxylic acid transport; intracellular chloride ion homeostasis; and mercury ion transport. Located in apical plasma membrane and intercellular canaliculus. Is expressed in foregut; genitourinary system; and liver and biliary system. Human ortholog(s) of this gene implicated in bile duct disease (multiple); bilirubin metabolic disorder (multiple); leukemia (multiple); liver disease (multiple); and lung non-small cell carcinoma. Orthologous to human ABCC2 (ATP binding cassette subfamily C member 2).