ATPase H+ transporting V0 subunit e1 pseudogene 2 (ATP6V0E1P2)

ATP6V0E1P2 is a human processed pseudogene located on chromosome 3[9], derived as a retrocopy of the ATP6V0E1 gene[7][9]. ATP6V0E1 itself encodes a V0 subunit e1 of the vacuolar ATPase (V-ATPase), an enzyme involved in proton transport across lysosomal and vacuolar membranes. However, ATP6V0E1P2 is a non-functional genomic element and does not produce a protein. While some pseudogenes have been shown to participate in gene regulation via their RNA transcripts, no regulatory or disease-related roles for ATP6V0E1P2 have been described in the literature or genetic databases. As such, it is not considered a molecular target for therapeutic intervention[1][3][4][5][7][8][9].\n\nATP6V0E1P2 is a pseudogene (non-coding, retrocopy) of ATP6V0E1, not a canonical therapeutic target, not associated with any known drug interactions, disease roles, or safety issues, and lacks an established biological function[1][3][4][5][7][8][9].

Other names

ATP6V0E1P2ATPase H+ transporting lysosomal 9kDa V0 subunit e1 pseudogene 2

None. There are no mechanisms of action described for ATP6V0E1P2, as it is not a drug target