Subunit a of the F0 sector of mitochondrial F1F0 ATP synthase; mitochondrially encoded; translation is specifically activated by Atp22p; ATP6 and ATP8 mRNAs are not translated in the absence of the F1 sector of ATPase; mutations in human ortholog MT-ATP6 are associated with neurodegenerative disorders such as Neurogenic Ataxia and Retinitis Pigmentosa (NARP), Leigh syndrome (LS), Charcot-Marie-Tooth (CMT), and ataxia telangiectasia [Source:SGD;Acc:S000007268]

OLI2, OLI4, PHO1

Chromosome Mito: 28,487-29,266 forward strand.

R64-1-1:AJ011856.1

This gene has 1 transcript (splice variant), 57 orthologues and is a member of 2 Ensembl protein families.

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