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]

IPP2

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

R64-1-1:BK006946.2

This gene has 1 transcript (splice variant), 124 orthologues, 1 paralogue and is a member of 1 Ensembl protein family.

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