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]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| TMEM199-20-RE | 20 (40 μL) | 200 μL |  |
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| TMEM199-20-OR | 20 (40 μL) | 200 μL |  |
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| TMEM199-20-GO | 20 (40 μL) | 200 μL |  |
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| TMEM199-20-GR | 20 (40 μL) | 200 μL |  |
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| TMEM199-20-AQ | 20 (40 μL) | 200 μL |  |
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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]
Gene Symbol : TMEM199
Gene Name : Transmembrane protein 199
Chromosome : CHR 17: 283,575,80-283,636,82
Locus : 17q11.2
Alt. Genes : KIF20A
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