XB-FEAT-5841560
(Redirected from Tmem199)
vma12
This is the community wiki page for the gene vma12 please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase
nomenclature updates
2025-02-07
Human and Xenopus gene names have changed, from tmem199 transmembrane protein 199, to vma12, vacuolar ATPase assembly factor VMA12 Approved by HGNC.
Summary for human gene VMA12 from NCBI
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) in some human cells. The encoded protein shares some homology with the yeast protein Vma12. Defects in this gene are a cause of congenital disorder of glycosylation, type IIp. [provided by RefSeq, Mar 2016]