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Torsin-1A-interacting protein 2 (TOR1AIP2) is a type II integral membrane protein primarily located in the endoplasmic reticulum (ER) and acts as a cofactor for the ATPase TorsinA, influencing its distribution between the ER and the nuclear envelope[1][9][8][2]. One isoform of the protein is responsive to interferon alpha, though its role in that context remains to be clarified[8]. TOR1AIP2 is implicated in maintaining ER integrity and modulating ATPase activity, and genetic defects in TOR1AIP2 are linked to neuromuscular disorders, including primary dystonia and specific myopathies[1][8]. There are no known drugs or therapeutic agents directly targeting this protein[1][9][8].
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