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.

This transcript has 1 exon, is annotated with 21 domains and features, is associated with 52 variant alleles and maps to 9 oligo probes.

This transcript is a product of gene Q0085 Show transcript tableHide transcript table