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MTATP6

Official Full Name
mitochondrially encoded ATP synthase 6
Organism
Homo sapiens
GeneID
4508
Background
Contributes to proton-transporting ATP synthase activity, rotational mechanism. Involved in proton motive force-driven mitochondrial ATP synthesis. Located in mitochondrion. Part of proton-transporting ATP synthase complex. Implicated in Leber hereditary optic neuropathy; NARP syndrome; Parkinson's disease; multiple sclerosis; and systemic lupus erythematosus. [provided by Alliance of Genome Resources, Feb 2025]
Synonyms
MT-ATP6; ATPase6; MTATP6; ATP6;

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