mitochondrially encoded ATP synthase membrane subunit 6
Synonyms
ATP synthase 6, mitochondrial
ATP synthase F0 subunit 6
Biotype
protein coding gene
Automated Description
Predicted to contribute to proton-transporting ATP synthase activity, rotational mechanism. Involved in response to hyperoxia. Predicted to be located in mitochondrion. Predicted to be part of proton-transporting ATP synthase complex, coupling factor F(o). Human ortholog(s) of this gene implicated in Leber hereditary optic neuropathy; NARP syndrome; Parkinson's disease; multiple sclerosis; and systemic lupus erythematosus. Orthologous to human MT-ATP6 (mitochondrially encoded ATP synthase membrane subunit 6).
RGD Description
Predicted to contribute to proton-transporting ATP synthase activity, rotational mechanism. Involved in response to hyperoxia. Predicted to be located in mitochondrion. Predicted to be part of proton-transporting ATP synthase complex, coupling factor F(o). Human ortholog(s) of this gene implicated in Leber hereditary optic neuropathy; NARP syndrome; Parkinson's disease; multiple sclerosis; and systemic lupus erythematosus. Orthologous to human MT-ATP6 (mitochondrially encoded ATP synthase membrane subunit 6); PARTICIPATES IN electron transport chain pathway; INTERACTS WITH 2,2',4,4'-Tetrabromodiphenyl ether; 2,3,7,8-tetrachlorodibenzodioxine; 3-chloropropane-1,2-diol.