COG5-FOXP1 Fusion FISH Probe
The COG5-FOXP1 Fusion FISH Probe is used to confirm a fusion of the COG5 and FOXP1 genes. The fusion of the COG5 and FOXP1 genes has been associated with Bladder Urothelial Carcinoma. These probes are FISH confirmed on normal peripheral blood in both interphase nuclei and metaphase spreads before shipment. Typical turnaround time for this product is 7-14 days after purchase.
** This product is for in vitro and research use only. This product is not intended for diagnostic use.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| COG5-FOXP1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| COG5-FOXP1-20-RERE | 20 (40 μL) | 200 μL |
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| COG5-FOXP1-20-REOR | 20 (40 μL) | 200 μL |
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| COG5-FOXP1-20-REGO | 20 (40 μL) | 200 μL |
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| COG5-FOXP1-20-REGR | 20 (40 μL) | 200 μL |
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| COG5-FOXP1-20-REAQ | 20 (40 μL) | 200 μL |
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| COG5-FOXP1-20-ORRE | 20 (40 μL) | 200 μL |
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| COG5-FOXP1-20-OROR | 20 (40 μL) | 200 μL |
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| COG5-FOXP1-20-ORGO | 20 (40 μL) | 200 μL |
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| COG5-FOXP1-20-ORAQ | 20 (40 μL) | 200 μL |
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| COG5-FOXP1-20-GORE | 20 (40 μL) | 200 μL |
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| COG5-FOXP1-20-GOOR | 20 (40 μL) | 200 μL |
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| COG5-FOXP1-20-GOGO | 20 (40 μL) | 200 μL |
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| COG5-FOXP1-20-GOGR | 20 (40 μL) | 200 μL |
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| COG5-FOXP1-20-GOAQ | 20 (40 μL) | 200 μL |
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| COG5-FOXP1-20-GRRE | 20 (40 μL) | 200 μL |
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| COG5-FOXP1-20-GROR | 20 (40 μL) | 200 μL |
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| COG5-FOXP1-20-GRGO | 20 (40 μL) | 200 μL |
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| COG5-FOXP1-20-GRGR | 20 (40 μL) | 200 μL |
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| COG5-FOXP1-20-GRAQ | 20 (40 μL) | 200 μL |
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| COG5-FOXP1-20-AQRE | 20 (40 μL) | 200 μL |
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| COG5-FOXP1-20-AQOR | 20 (40 μL) | 200 μL |
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| COG5-FOXP1-20-AQGO | 20 (40 μL) | 200 μL |
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| COG5-FOXP1-20-AQGR | 20 (40 μL) | 200 μL |
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| COG5-FOXP1-20-AQAQ | 20 (40 μL) | 200 μL |
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COG5 Gene Summary
The protein encoded by this gene is one of eight proteins (Cog1-8) which form a Golgi-localized complex (COG) required for normal Golgi morphology and function. The encoded protein is organized with conserved oligomeric Golgi complex components 6, 7 and 8 into a sub-complex referred to as lobe B. Alternative splicing results in multiple transcript variants. Mutations in this gene result in congenital disorder of glycosylation type 2I.[provided by RefSeq, Jan 2011]
Gene Name: Component Of Oligomeric Golgi Complex 5
Chromosome: CHR7: 106842188 -107204959
Locus: 7q22.3
FOXP1 Gene Summary
This gene belongs to subfamily P of the forkhead box (FOX) transcription factor family. Forkhead box transcription factors play important roles in the regulation of tissue- and cell type-specific gene transcription during both development and adulthood. Forkhead box P1 protein contains both DNA-binding- and protein-protein binding-domains. This gene may act as a tumor suppressor as it is lost in several tumor types and maps to a chromosomal region (3p14.1) reported to contain a tumor suppressor gene(s). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]
Gene Name: Forkhead Box P1
Chromosome: CHR3: 71004735 -71633140
Locus: 3p13
Gene Diseases
The COG5 FOXP1 Fusion has been associated with the following diseases:
| Disease Name |
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| Bladder Urothelial Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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