This gene encodes a protein that is a component of the conserved oligomeric Golgi (COG) complex, a multiprotein complex that plays a structural role in the Golgi apparatus, and is involved in intracellular membrane trafficking and glycoprotein modification. Mutations in this gene cause congenital disorder of glycosylation, type IIh, a disease that is characterized by under-glycosylated serum proteins, and whose symptoms include severe psychomotor retardation, failure to thrive, seizures, and dairy and wheat product intolerance. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| COG8-20-RE | 20 (40 μL) | 200 μL |  |
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| COG8-20-OR | 20 (40 μL) | 200 μL |  |
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| COG8-20-GO | 20 (40 μL) | 200 μL |  |
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| COG8-20-GR | 20 (40 μL) | 200 μL |  |
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| COG8-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a protein that is a component of the conserved oligomeric Golgi (COG) complex, a multiprotein complex that plays a structural role in the Golgi apparatus, and is involved in intracellular membrane trafficking and glycoprotein modification. Mutations in this gene cause congenital disorder of glycosylation, type IIh, a disease that is characterized by under-glycosylated serum proteins, and whose symptoms include severe psychomotor retardation, failure to thrive, seizures, and dairy and wheat product intolerance. [provided by RefSeq, Jul 2008]
Gene Symbol : COG8
Gene Name : Component of oligomeric golgi complex 8
Chromosome : CHR 16: 693,396,22-693,286,20
Locus : 16q22.1
Alt. Genes : FEM1B
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