CPRiL

Abcb1a

ATP binding cassette subfamily B member 1A

Predicted to enable several functions, including ATP binding activity; ATP hydrolysis activity; and ATPase-coupled intramembrane lipid transporter activity. Involved in several processes, including cellular hyperosmotic salinity response; cellular response to L-glutamate; and cellular response to borneol. Located in brush border membrane. Biomarker of brain disease (multiple); end stage renal disease; human immunodeficiency virus infectious disease; liver disease (multiple); and obstructive sleep apnea. Human ortholog(s) of this gene implicated in several diseases, including carcinoma (multiple); drug dependence (multiple); human immunodeficiency virus infectious disease (multiple); inflammatory bowel disease (multiple); and leukemia (multiple). Orthologous to human ABCB1 (ATP binding cassette subfamily B member 1). [provided by Alliance of Genome Resources, Jun 2025]

• ATP binding cassette subfamily B member 1A
• ATP binding cassette subfamily B member 1
• ATP-binding cassette, sub-family B (MDR/TAP), member 1
ATP-binding cassette, sub-family B (MDR/TAP), member 1A
ATP-binding cassette, subfamily B (MDR/TAP), member 1A
multiple drug resistant 1a
Abcb1
Mdr1a