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), 843 orthologues and 1 paralogue.

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