SYTL3-SNX9 Fusion FISH Probe
The SYTL3-SNX9 Fusion FISH Probe is used to confirm a fusion of the SYTL3 and SNX9 genes. The fusion of the SYTL3 and SNX9 genes has been associated with Uterine Corpus Endometrial 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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SYTL3-SNX9-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
SYTL3-SNX9-20-RERE | 20 (40 μL) | 200 μL | ||
SYTL3-SNX9-20-REOR | 20 (40 μL) | 200 μL | ||
SYTL3-SNX9-20-REGO | 20 (40 μL) | 200 μL | ||
SYTL3-SNX9-20-REGR | 20 (40 μL) | 200 μL | ||
SYTL3-SNX9-20-REAQ | 20 (40 μL) | 200 μL | ||
SYTL3-SNX9-20-ORRE | 20 (40 μL) | 200 μL | ||
SYTL3-SNX9-20-OROR | 20 (40 μL) | 200 μL | ||
SYTL3-SNX9-20-ORGO | 20 (40 μL) | 200 μL | ||
SYTL3-SNX9-20-ORAQ | 20 (40 μL) | 200 μL | ||
SYTL3-SNX9-20-GORE | 20 (40 μL) | 200 μL | ||
SYTL3-SNX9-20-GOOR | 20 (40 μL) | 200 μL | ||
SYTL3-SNX9-20-GOGO | 20 (40 μL) | 200 μL | ||
SYTL3-SNX9-20-GOGR | 20 (40 μL) | 200 μL | ||
SYTL3-SNX9-20-GOAQ | 20 (40 μL) | 200 μL | ||
SYTL3-SNX9-20-GRRE | 20 (40 μL) | 200 μL | ||
SYTL3-SNX9-20-GROR | 20 (40 μL) | 200 μL | ||
SYTL3-SNX9-20-GRGO | 20 (40 μL) | 200 μL | ||
SYTL3-SNX9-20-GRGR | 20 (40 μL) | 200 μL | ||
SYTL3-SNX9-20-GRAQ | 20 (40 μL) | 200 μL | ||
SYTL3-SNX9-20-AQRE | 20 (40 μL) | 200 μL | ||
SYTL3-SNX9-20-AQOR | 20 (40 μL) | 200 μL | ||
SYTL3-SNX9-20-AQGO | 20 (40 μL) | 200 μL | ||
SYTL3-SNX9-20-AQGR | 20 (40 μL) | 200 μL | ||
SYTL3-SNX9-20-AQAQ | 20 (40 μL) | 200 μL |
SNX9 Gene Summary
This gene encodes a member of the sorting nexin family. Members of this family contain a phosphoinositide binding domain, and are involved in intracellular trafficking. The encoded protein does not contain a coiled coil region, like some family members, but does contain a SRC homology domain near its N-terminus. The encoded protein is reported to have a variety of interaction partners, including of adaptor protein 2 , dynamin, tyrosine kinase non-receptor 2, Wiskott-Aldrich syndrome-like, and ARP3 actin-related protein 3. The encoded protein is implicated in several stages of intracellular trafficking, including endocytosis, macropinocytosis, and F-actin nucleation. [provided by RefSeq, Jul 2013]
Gene Name: Sorting Nexin 9
Chromosome: CHR6: 158244293 -158366109
Locus: 6q25.3
SYTL3 Gene Summary
The protein encoded by this gene belongs to a family of peripheral membrane proteins that play a role in vesicular trafficking. This protein binds phospholipids in the presence of calcium ions. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2016]
Gene Name: Synaptotagmin Like 3
Chromosome: CHR6: 159071045 -159185908
Locus: 6q25.3
Gene Diseases
The SYTL3 SNX9 Fusion has been associated with the following diseases:
Disease Name |
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Uterine Corpus Endometrial Carcinoma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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