Vacuolar ATPase assembly protein VMA22 is a protein that in humans is encoded by the VMA22 gene (formerly CCDC115).
Function The protein encoded by this gene has been observed to localize to the endoplasmic reticulum (ER)-Golgi intermediate compartment (ERGIC) and coat protein complex I (COPI) vesicles in some human cells. The encoded protein shares some homology with the yeast V-ATPase assembly factor Vma22p, and the orthologous protein in mouse promotes cell proliferation and suppresses cell death. Defects in this gene are a cause of congenital disorder of glycosylation, type IIo in humans. [provided by RefSeq, Mar 2016].
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This article incorporates text from the United States National Library of Medicine, which is in the public domain.





