C5ORF42-SEMA5A Fusion FISH Probe
The C5ORF42-SEMA5A Fusion FISH Probe is used to confirm a fusion of the C5ORF42 and SEMA5A genes. The fusion of the C5ORF42 and SEMA5A genes has been associated with Skin Cutaneous Melanoma. 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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| C5ORF42-SEMA5A-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| C5ORF42-SEMA5A-20-RERE | 20 (40 μL) | 200 μL |
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| C5ORF42-SEMA5A-20-REOR | 20 (40 μL) | 200 μL |
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| C5ORF42-SEMA5A-20-REGO | 20 (40 μL) | 200 μL |
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| C5ORF42-SEMA5A-20-REGR | 20 (40 μL) | 200 μL |
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| C5ORF42-SEMA5A-20-REAQ | 20 (40 μL) | 200 μL |
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| C5ORF42-SEMA5A-20-ORRE | 20 (40 μL) | 200 μL |
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| C5ORF42-SEMA5A-20-OROR | 20 (40 μL) | 200 μL |
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| C5ORF42-SEMA5A-20-ORGO | 20 (40 μL) | 200 μL |
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| C5ORF42-SEMA5A-20-ORAQ | 20 (40 μL) | 200 μL |
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| C5ORF42-SEMA5A-20-GORE | 20 (40 μL) | 200 μL |
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| C5ORF42-SEMA5A-20-GOOR | 20 (40 μL) | 200 μL |
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| C5ORF42-SEMA5A-20-GOGO | 20 (40 μL) | 200 μL |
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| C5ORF42-SEMA5A-20-GOGR | 20 (40 μL) | 200 μL |
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| C5ORF42-SEMA5A-20-GOAQ | 20 (40 μL) | 200 μL |
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| C5ORF42-SEMA5A-20-GRRE | 20 (40 μL) | 200 μL |
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| C5ORF42-SEMA5A-20-GROR | 20 (40 μL) | 200 μL |
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| C5ORF42-SEMA5A-20-GRGO | 20 (40 μL) | 200 μL |
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| C5ORF42-SEMA5A-20-GRGR | 20 (40 μL) | 200 μL |
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| C5ORF42-SEMA5A-20-GRAQ | 20 (40 μL) | 200 μL |
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| C5ORF42-SEMA5A-20-AQRE | 20 (40 μL) | 200 μL |
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| C5ORF42-SEMA5A-20-AQOR | 20 (40 μL) | 200 μL |
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| C5ORF42-SEMA5A-20-AQGO | 20 (40 μL) | 200 μL |
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| C5ORF42-SEMA5A-20-AQGR | 20 (40 μL) | 200 μL |
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| C5ORF42-SEMA5A-20-AQAQ | 20 (40 μL) | 200 μL |
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SEMA5A Gene Summary
This gene belongs to the semaphorin gene family that encodes membrane proteins containing a semaphorin domain and several thrombospondin type-1 repeats. Members of this family are involved in axonal guidance during neural development. This gene has been implicated as an autism susceptibility gene.[provided by RefSeq, Jan 2010]
Gene Name: Semaphorin 5A
Chromosome: CHR5: 9035137 -9546233
Locus: 5p15.31
C5orf42 Gene Summary
The protein encoded by this gene has putative coiled-coil domains and may be a transmembrane protein. Defects in this gene are a cause of Joubert syndrome (JBTS). [provided by RefSeq, May 2012]
Gene Name: Chromosome 5 Open Reading Frame 42
Chromosome: CHR5: 37106329 -37249530
Locus: 5p13.2
Gene Diseases
The C5ORF42 SEMA5A Fusion has been associated with the following diseases:
| Disease Name |
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| Skin Cutaneous Melanoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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