The protein encoded by this gene resides in the golgi, and constitutes one of the 8 subunits of the conserved oligomeric Golgi (COG) complex, which is required for normal golgi morphology and localization. Mutations in this gene are associated with the congenital disorder of glycosylation type IIe.[provided by RefSeq, May 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| COG7-20-RE | 20 (40 μL) | 200 μL |  |
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| COG7-20-OR | 20 (40 μL) | 200 μL |  |
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| COG7-20-GO | 20 (40 μL) | 200 μL |  |
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| COG7-20-GR | 20 (40 μL) | 200 μL |  |
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| COG7-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene resides in the golgi, and constitutes one of the 8 subunits of the conserved oligomeric Golgi (COG) complex, which is required for normal golgi morphology and localization. Mutations in this gene are associated with the congenital disorder of glycosylation type IIe.[provided by RefSeq, May 2010]
Gene Symbol : COG7
Gene Name : Component of oligomeric golgi complex 7
Chromosome : CHR 16: 234,532,14-233,884,92
Locus : 16p12.2
Alt. Genes : ZNF263
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