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GTF2IRD1-CLIP2 Fusion FISH Probe

The GTF2IRD1-CLIP2 Fusion FISH Probe is used to confirm a fusion of the GTF2IRD1 and CLIP2 genes. The fusion of the GTF2IRD1 and CLIP2 genes has been associated with Uterine Carcinosarcoma. 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.

Turnaround Time: 7-10 Business Days    Shipping Time: 1-2 Day Expedited Shipping

SKU Test Kits Buffer Dye Color Order Now
GTF2IRD1-CLIP2-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
GTF2IRD1-CLIP2-20-RERE 20 (40 μL) 200 μL
GTF2IRD1-CLIP2-20-REOR 20 (40 μL) 200 μL
GTF2IRD1-CLIP2-20-REGO 20 (40 μL) 200 μL
GTF2IRD1-CLIP2-20-REGR 20 (40 μL) 200 μL
GTF2IRD1-CLIP2-20-REAQ 20 (40 μL) 200 μL
GTF2IRD1-CLIP2-20-ORRE 20 (40 μL) 200 μL
GTF2IRD1-CLIP2-20-OROR 20 (40 μL) 200 μL
GTF2IRD1-CLIP2-20-ORGO 20 (40 μL) 200 μL
GTF2IRD1-CLIP2-20-ORAQ 20 (40 μL) 200 μL
GTF2IRD1-CLIP2-20-GORE 20 (40 μL) 200 μL
GTF2IRD1-CLIP2-20-GOOR 20 (40 μL) 200 μL
GTF2IRD1-CLIP2-20-GOGO 20 (40 μL) 200 μL
GTF2IRD1-CLIP2-20-GOGR 20 (40 μL) 200 μL
GTF2IRD1-CLIP2-20-GOAQ 20 (40 μL) 200 μL
GTF2IRD1-CLIP2-20-GRRE 20 (40 μL) 200 μL
GTF2IRD1-CLIP2-20-GROR 20 (40 μL) 200 μL
GTF2IRD1-CLIP2-20-GRGO 20 (40 μL) 200 μL
GTF2IRD1-CLIP2-20-GRGR 20 (40 μL) 200 μL
GTF2IRD1-CLIP2-20-GRAQ 20 (40 μL) 200 μL
GTF2IRD1-CLIP2-20-AQRE 20 (40 μL) 200 μL
GTF2IRD1-CLIP2-20-AQOR 20 (40 μL) 200 μL
GTF2IRD1-CLIP2-20-AQGO 20 (40 μL) 200 μL
GTF2IRD1-CLIP2-20-AQGR 20 (40 μL) 200 μL
GTF2IRD1-CLIP2-20-AQAQ 20 (40 μL) 200 μL

CLIP2 Gene Summary

The protein encoded by this gene belongs to the family of cytoplasmic linker proteins, which have been proposed to mediate the interaction between specific membranous organelles and microtubules. This protein was found to associate with both microtubules and an organelle called the dendritic lamellar body. This gene is hemizygously deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants. [provided by RefSeq, Jul 2008]

Gene Name: CAP-Gly Domain Containing Linker Protein 2

Chromosome: CHR7: 73703804 -73820273

Locus: 7q11.23

GTF2IRD1 Gene Summary

The protein encoded by this gene contains five GTF2I-like repeats and each repeat possesses a potential helix-loop-helix (HLH) motif. It may have the ability to interact with other HLH-proteins and function as a transcription factor or as a positive transcriptional regulator under the control of Retinoblastoma protein. This gene plays a role in craniofacial and cognitive development and mutations have been associated with Williams-Beuren syndrome, a multisystem developmental disorder caused by deletion of multiple genes at 7q11.23. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2010]

Gene Name: GTF2I Repeat Domain Containing 1

Chromosome: CHR7: 73868119 -74016920

Locus: 7q11.23

Gene Diseases

The GTF2IRD1 CLIP2 Fusion has been associated with the following diseases:

Disease Name
Uterine Carcinosarcoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.