LRRC6-EXT1 Fusion FISH Probe
The LRRC6-EXT1 Fusion FISH Probe is used to confirm a fusion of the LRRC6 and EXT1 genes. The fusion of the LRRC6 and EXT1 genes has been associated with Breast Invasive 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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| LRRC6-EXT1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| LRRC6-EXT1-20-RERE | 20 (40 μL) | 200 μL |
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| LRRC6-EXT1-20-REOR | 20 (40 μL) | 200 μL |
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| LRRC6-EXT1-20-REGO | 20 (40 μL) | 200 μL |
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| LRRC6-EXT1-20-REGR | 20 (40 μL) | 200 μL |
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| LRRC6-EXT1-20-REAQ | 20 (40 μL) | 200 μL |
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| LRRC6-EXT1-20-ORRE | 20 (40 μL) | 200 μL |
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| LRRC6-EXT1-20-OROR | 20 (40 μL) | 200 μL |
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| LRRC6-EXT1-20-ORGO | 20 (40 μL) | 200 μL |
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| LRRC6-EXT1-20-ORAQ | 20 (40 μL) | 200 μL |
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| LRRC6-EXT1-20-GORE | 20 (40 μL) | 200 μL |
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| LRRC6-EXT1-20-GOOR | 20 (40 μL) | 200 μL |
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| LRRC6-EXT1-20-GOGO | 20 (40 μL) | 200 μL |
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| LRRC6-EXT1-20-GOGR | 20 (40 μL) | 200 μL |
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| LRRC6-EXT1-20-GOAQ | 20 (40 μL) | 200 μL |
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| LRRC6-EXT1-20-GRRE | 20 (40 μL) | 200 μL |
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| LRRC6-EXT1-20-GROR | 20 (40 μL) | 200 μL |
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| LRRC6-EXT1-20-GRGO | 20 (40 μL) | 200 μL |
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| LRRC6-EXT1-20-GRGR | 20 (40 μL) | 200 μL |
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| LRRC6-EXT1-20-GRAQ | 20 (40 μL) | 200 μL |
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| LRRC6-EXT1-20-AQRE | 20 (40 μL) | 200 μL |
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| LRRC6-EXT1-20-AQOR | 20 (40 μL) | 200 μL |
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| LRRC6-EXT1-20-AQGO | 20 (40 μL) | 200 μL |
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| LRRC6-EXT1-20-AQGR | 20 (40 μL) | 200 μL |
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| LRRC6-EXT1-20-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
LRRC6 Gene Summary
The protein encoded by this gene contains several leucine-rich repeat domains and appears to be involved in the motility of cilia. Defects in this gene are a cause of primary ciliary dyskinesia-19 (CILD19). Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 4, 11 and 22. [provided by RefSeq, Apr 2016]
Gene Name: Leucine Rich Repeat Containing 6
Chromosome: CHR8: 133584446 -133687813
Locus: 8q24.22
Gene Diseases
The LRRC6 EXT1 Fusion has been associated with the following diseases:
| Disease Name |
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| Breast Invasive Carcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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