Mitochondrially encoded ATP synthase 6 pseudogene 11 (MTATP6P11)

MTATP6P11 is one of several pseudogenes related to the MT-ATP6 gene, which encodes a subunit (subunit a) of the mitochondrial ATP synthase (Complex V, responsible for ATP generation via oxidative phosphorylation) in its functional form[1][4]. As a pseudogene, MTATP6P11 does not encode a protein and is not believed to produce any functional RNA or protein products. There is no current evidence linking MTATP6P11 to any biological functions, disease states, or therapeutic targeting[2][4]. It is found in genomic databases as a nonfunctional genomic element, and is not listed in clinical, disease association, or drug target panels. The functional MT-ATP6 gene (not the pseudogene) is involved in mitochondrial ATP production and is associated with rare mitochondrial diseases when mutated, such as Leigh syndrome[1][7]. MTATP6P11, as a pseudogene, is unrelated to these disorders and does not share their functional or clinical significance. There are no known biomarkers, safety concerns, disease associations, or drugs associated with this pseudogene.

Other names

MT-ATP6 pseudogene 11MTATP6P11mitochondrially encoded ATP synthase 6 pseudogene 11