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GRHL2-CRMP1 Fusion FISH Probe

The GRHL2-CRMP1 Fusion FISH Probe is used to confirm a fusion of the GRHL2 and CRMP1 genes. The fusion of the GRHL2 and CRMP1 genes has been associated with Head And Neck Squamous Cell 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.

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

SKU Test Kits Buffer Dye Color Order Now
GRHL2-CRMP1-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
GRHL2-CRMP1-20-RERE 20 (40 μL) 200 μL
GRHL2-CRMP1-20-REOR 20 (40 μL) 200 μL
GRHL2-CRMP1-20-REGO 20 (40 μL) 200 μL
GRHL2-CRMP1-20-REGR 20 (40 μL) 200 μL
GRHL2-CRMP1-20-REAQ 20 (40 μL) 200 μL
GRHL2-CRMP1-20-ORRE 20 (40 μL) 200 μL
GRHL2-CRMP1-20-OROR 20 (40 μL) 200 μL
GRHL2-CRMP1-20-ORGO 20 (40 μL) 200 μL
GRHL2-CRMP1-20-ORAQ 20 (40 μL) 200 μL
GRHL2-CRMP1-20-GORE 20 (40 μL) 200 μL
GRHL2-CRMP1-20-GOOR 20 (40 μL) 200 μL
GRHL2-CRMP1-20-GOGO 20 (40 μL) 200 μL
GRHL2-CRMP1-20-GOGR 20 (40 μL) 200 μL
GRHL2-CRMP1-20-GOAQ 20 (40 μL) 200 μL
GRHL2-CRMP1-20-GRRE 20 (40 μL) 200 μL
GRHL2-CRMP1-20-GROR 20 (40 μL) 200 μL
GRHL2-CRMP1-20-GRGO 20 (40 μL) 200 μL
GRHL2-CRMP1-20-GRGR 20 (40 μL) 200 μL
GRHL2-CRMP1-20-GRAQ 20 (40 μL) 200 μL
GRHL2-CRMP1-20-AQRE 20 (40 μL) 200 μL
GRHL2-CRMP1-20-AQOR 20 (40 μL) 200 μL
GRHL2-CRMP1-20-AQGO 20 (40 μL) 200 μL
GRHL2-CRMP1-20-AQGR 20 (40 μL) 200 μL
GRHL2-CRMP1-20-AQAQ 20 (40 μL) 200 μL

CRMP1 Gene Summary

This gene encodes a member of a family of cytosolic phosphoproteins expressed exclusively in the nervous system. The encoded protein is thought to be a part of the semaphorin signal transduction pathway implicated in semaphorin-induced growth cone collapse during neural development. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]

Gene Name: Collapsin Response Mediator Protein 1

Chromosome: CHR4: 5822490 -5894785

Locus: 4p16.2

GRHL2 Gene Summary

The protein encoded by this gene is a transcription factor that can act as a homodimer or as a heterodimer with either GRHL1 or GRHL3. Defects in this gene are a cause of non-syndromic sensorineural deafness autosomal dominant type 28 (DFNA28).[provided by RefSeq, Mar 2009]

Gene Name: Grainyhead Like Transcription Factor 2

Chromosome: CHR8: 102504667 -102681952

Locus: 8q22.3

Gene Diseases

The GRHL2 CRMP1 Fusion has been associated with the following diseases:

Disease Name
Head And Neck Squamous Cell Carcinoma 

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.