Ornithine transporter of the mitochondrial inner membrane; exports ornithine from mitochondria as part of arginine biosynthesis; functionally complemented by human ortholog, SLC25A15, which is associated with hyperammonaemia-hyperornithinaemia-homocitrullinuria (HHH) syndrome, but HHH-associated variants fail to complement [Source:SGD;Acc:S000005656]
ARG11
Chromosome XV: 569,929-570,807 reverse strand.
R64-1-1:BK006948.2
This gene has 1 transcript (splice variant), 389 orthologues and 34 paralogues.