| Gene Symbol | TMEM199 |
| Entrez Gene ID | 147007 |
| Full Name | transmembrane protein 199 |
| Synonyms | C17orf32,CDG2P,VMA12,VPH2 |
| General protein information |
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| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| 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. [provided by RefSeq, Mar 2016]. |
| Disorder MIM: | |
| Disorder Html: | Congenital disorder of glycosylation, type IIp, 616829 (3) |
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