EXT1-WDYHV1 Fusion FISH Probe
The EXT1-WDYHV1 Fusion FISH Probe is used to confirm a fusion of the EXT1 and WDYHV1 genes. The fusion of the EXT1 and WDYHV1 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. Please note that both genes fall on the same chromosome and inter-chromosomal detection may be difficult to detect depending on the genes proximity to one another. Please consult our support staff before ordering this product to ensure that the probe can be designed to meet your specific needs.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| EXT1-WDYHV1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| EXT1-WDYHV1-20-RERE | 20 (40 μL) | 200 μL |
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| EXT1-WDYHV1-20-REOR | 20 (40 μL) | 200 μL |
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| EXT1-WDYHV1-20-REGO | 20 (40 μL) | 200 μL |
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| EXT1-WDYHV1-20-REGR | 20 (40 μL) | 200 μL |
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| EXT1-WDYHV1-20-REAQ | 20 (40 μL) | 200 μL |
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| EXT1-WDYHV1-20-ORRE | 20 (40 μL) | 200 μL |
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| EXT1-WDYHV1-20-OROR | 20 (40 μL) | 200 μL |
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| EXT1-WDYHV1-20-ORGO | 20 (40 μL) | 200 μL |
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| EXT1-WDYHV1-20-ORAQ | 20 (40 μL) | 200 μL |
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| EXT1-WDYHV1-20-GORE | 20 (40 μL) | 200 μL |
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| EXT1-WDYHV1-20-GOOR | 20 (40 μL) | 200 μL |
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| EXT1-WDYHV1-20-GOGO | 20 (40 μL) | 200 μL |
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| EXT1-WDYHV1-20-GOGR | 20 (40 μL) | 200 μL |
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| EXT1-WDYHV1-20-GOAQ | 20 (40 μL) | 200 μL |
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| EXT1-WDYHV1-20-GRRE | 20 (40 μL) | 200 μL |
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| EXT1-WDYHV1-20-GROR | 20 (40 μL) | 200 μL |
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| EXT1-WDYHV1-20-GRGO | 20 (40 μL) | 200 μL |
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| EXT1-WDYHV1-20-GRGR | 20 (40 μL) | 200 μL |
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| EXT1-WDYHV1-20-GRAQ | 20 (40 μL) | 200 μL |
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| EXT1-WDYHV1-20-AQRE | 20 (40 μL) | 200 μL |
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| EXT1-WDYHV1-20-AQOR | 20 (40 μL) | 200 μL |
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| EXT1-WDYHV1-20-AQGO | 20 (40 μL) | 200 μL |
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| EXT1-WDYHV1-20-AQGR | 20 (40 μL) | 200 μL |
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| EXT1-WDYHV1-20-AQAQ | 20 (40 μL) | 200 μL |
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EXT1 Gene Summary
This gene encodes an endoplasmic reticulum-resident type II transmembrane glycosyltransferase involved in the chain elongation step of heparan sulfate biosynthesis. Mutations in this gene cause the type I form of multiple exostoses. [provided by RefSeq, Jul 2008]
Gene Name: Exostosin Glycosyltransferase 1
Chromosome: CHR8: 118811601 -119124058
Locus: 8q24.11
WDYHV1 Gene Summary
The WDYHV Motif Containing 1 (WDYHV1) gene is located on chr8 :124428964-124454260 at 8q24.13.
Gene Name: WDYHV Motif Containing 1
Chromosome: CHR8: 124428964 -124454260
Locus: 8q24.13
Gene Diseases
The EXT1 WDYHV1 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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