Automated description from the Alliance of Genome Resources
Predicted to have several functions, including ATP binding activity; protein homodimerization activity; and protein self-association. Predicted to be involved in fatty acid metabolic process and peroxisome organization. Localizes to the peroxisomal membrane. Used to study congenital bile acid synthesis defect 5. Human ortholog(s) of this gene implicated in Zellweger syndrome and congenital bile acid synthesis defect 5. Is expressed in several structures, including alimentary system; brain; cardiovascular system; genitourinary system; and sensory organ. Orthologous to human ABCD3 (ATP binding cassette subfamily D member 3).