Mitochondrial inorganic pyrophosphatase; required for mitochondrial function and possibly involved in energy generation from inorganic pyrophosphate; human ortholog, PPA2, functionally complements the null mutant; mutations in human PPA2 cause a mitochondrial disease resulting in sudden unexpected cardiac arrest in infants [Source:SGD;Acc:S000004880]

Chromosome XIII: 801,772-802,704 forward strand.

This transcript has 1 exon, is annotated with 7 domains and features, is associated with 46 variant alleles and maps to 29 oligo probes.

This transcript is a product of gene YMR267W Show transcript tableHide transcript table