Subunit of heterodimeric peroxisomal ABC transport complex, with Pxa2p; required for import of long-chain fatty acids into peroxisomes; similar to human adrenoleukodystrophy transporters ABCD1and ABCD2, and ALD-related proteins; mutations in ABCD1 cause X-linked adrenoleukodystrophy (X-ALD), a peroxisomal disorder; human ABCD1 and ABCD2 can each partially complement yeast pxa1 pxa2 double null mutant [Source:SGD;Acc:S000006068]
LPI1, PAL1, PAT2, SSH2
Chromosome XVI: 273,255-275,867 forward strand.
R64-1-1:BK006949.2
This gene has 1 transcript (splice variant), 352 orthologues and 1 paralogue.