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TMEM199

Official Full Name
transmembrane protein 199
Organism
Homo sapiens
GeneID
147007
Background
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]
Synonyms
VPH2; CDG2P; VMA12; C17orf32;

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