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RNGTT-AHI1 Fusion FISH Probe

The RNGTT-AHI1 Fusion FISH Probe is used to confirm a fusion of the RNGTT and AHI1 genes. The fusion of the RNGTT and AHI1 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.

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

SKU Test Kits Buffer Dye Color Order Now
RNGTT-AHI1-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
RNGTT-AHI1-20-RERE 20 (40 μL) 200 μL
RNGTT-AHI1-20-REOR 20 (40 μL) 200 μL
RNGTT-AHI1-20-REGO 20 (40 μL) 200 μL
RNGTT-AHI1-20-REGR 20 (40 μL) 200 μL
RNGTT-AHI1-20-REAQ 20 (40 μL) 200 μL
RNGTT-AHI1-20-ORRE 20 (40 μL) 200 μL
RNGTT-AHI1-20-OROR 20 (40 μL) 200 μL
RNGTT-AHI1-20-ORGO 20 (40 μL) 200 μL
RNGTT-AHI1-20-ORAQ 20 (40 μL) 200 μL
RNGTT-AHI1-20-GORE 20 (40 μL) 200 μL
RNGTT-AHI1-20-GOOR 20 (40 μL) 200 μL
RNGTT-AHI1-20-GOGO 20 (40 μL) 200 μL
RNGTT-AHI1-20-GOGR 20 (40 μL) 200 μL
RNGTT-AHI1-20-GOAQ 20 (40 μL) 200 μL
RNGTT-AHI1-20-GRRE 20 (40 μL) 200 μL
RNGTT-AHI1-20-GROR 20 (40 μL) 200 μL
RNGTT-AHI1-20-GRGO 20 (40 μL) 200 μL
RNGTT-AHI1-20-GRGR 20 (40 μL) 200 μL
RNGTT-AHI1-20-GRAQ 20 (40 μL) 200 μL
RNGTT-AHI1-20-AQRE 20 (40 μL) 200 μL
RNGTT-AHI1-20-AQOR 20 (40 μL) 200 μL
RNGTT-AHI1-20-AQGO 20 (40 μL) 200 μL
RNGTT-AHI1-20-AQGR 20 (40 μL) 200 μL
RNGTT-AHI1-20-AQAQ 20 (40 μL) 200 μL

RNGTT Gene Summary

The RNA Guanylyltransferase And 5'-phosphatase (RNGTT) gene is located on chr6 :89319988-89673348 at 6q15.

Gene Name: RNA Guanylyltransferase And 5'-phosphatase

Chromosome: CHR6: 89319988 -89673348

Locus: 6q15

AHI1 Gene Summary

This gene is apparently required for both cerebellar and cortical development in humans. This gene mutations cause specific forms of Joubert syndrome-related disorders. Joubert syndrome (JS) is a recessively inherited developmental brain disorder with several identified causative chromosomal loci. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Oct 2008]

Gene Name: Abelson Helper Integration Site 1

Chromosome: CHR6: 135605109 -135818903

Locus: 6q23.3

Gene Diseases

The RNGTT AHI1 Fusion has been associated with the following diseases:

Disease Name
Skin Cutaneous Melanoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.