| Protein Name | vacuolar ATPase assembly factor VMA22 |
|---|---|
| Organism | Homo sapiens |
| Gene ID | 84317 |
| Gene Symbol | VMA22 |
| UniProt | Q96NT0 (CC115_HUMAN), B8ZZ99 (B8ZZ99_HUMAN), A1QKJ6 (A1QKJ6_HUMAN) |
| Relationships |
Total Number of functionally related compound(s) :
30
Total Number of Articles : 17 |
Description |
vacuolar ATPase assembly factor VMA22 |
| Gene Summary |
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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