Gene: TMEM199

Alternate names for this Gene: C17orf32|CDG2P|VMA12|VPH2

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) 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.

Gene is located in Chromosome: 17

Location in Chromosome : 17q11.2

Description of this Gene: transmembrane protein 199

Type of Gene: protein-coding