{"symbol":"VMA22","synonyms":[],"name":"vacuolar ATPase assembly factor VMA22","description":"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]","ncbiEntrezGeneId":84317,"ncbiEntrezGeneUrl":"https://ncbi.nlm.nih.gov/gene/84317","proteins":[],"hgncRootFamilies":[]}