The protein encoded by this gene is a component of an oligomeric protein complex involved in the structure and function of the Golgi apparatus. Defects in this gene may be a cause of congenital disorder of glycosylation type IIj. Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Aug 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| COG4-20-RE | 20 (40 μL) | 200 μL |  |
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| COG4-20-OR | 20 (40 μL) | 200 μL |  |
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| COG4-20-GO | 20 (40 μL) | 200 μL |  |
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| COG4-20-GR | 20 (40 μL) | 200 μL |  |
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| COG4-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene is a component of an oligomeric protein complex involved in the structure and function of the Golgi apparatus. Defects in this gene may be a cause of congenital disorder of glycosylation type IIj. Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Aug 2010]
Gene Symbol : COG4
Gene Name : Component of oligomeric golgi complex 4
Chromosome : CHR 16: 705,235,53-704,805,68
Locus : 16q22.1
Alt. Genes : PREB
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