{"symbol":"TMEM199","synonyms":["VMA12","VPH2","C17ORF32","CDG2P"],"name":"transmembrane protein 199","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) 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]","ncbiEntrezGeneId":147007,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/147007","proteins":[{"symbol":"TM199_HUMAN","href":"/api/1.0/protein/TM199_HUMAN"}],"hgncRootFamilies":[]}