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LYRM4-FARS2 Fusion FISH Probe

The LYRM4-FARS2 Fusion FISH Probe is used to confirm a fusion of the LYRM4 and FARS2 genes. The fusion of the LYRM4 and FARS2 genes has been associated with Skin Cutaneous Melanoma, and Cervical Squamous Cell Carcinoma And Endocervical Adenocarcinoma. 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
LYRM4-FARS2-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
LYRM4-FARS2-20-RERE 20 (40 μL) 200 μL
LYRM4-FARS2-20-REOR 20 (40 μL) 200 μL
LYRM4-FARS2-20-REGO 20 (40 μL) 200 μL
LYRM4-FARS2-20-REGR 20 (40 μL) 200 μL
LYRM4-FARS2-20-REAQ 20 (40 μL) 200 μL
LYRM4-FARS2-20-ORRE 20 (40 μL) 200 μL
LYRM4-FARS2-20-OROR 20 (40 μL) 200 μL
LYRM4-FARS2-20-ORGO 20 (40 μL) 200 μL
LYRM4-FARS2-20-ORAQ 20 (40 μL) 200 μL
LYRM4-FARS2-20-GORE 20 (40 μL) 200 μL
LYRM4-FARS2-20-GOOR 20 (40 μL) 200 μL
LYRM4-FARS2-20-GOGO 20 (40 μL) 200 μL
LYRM4-FARS2-20-GOGR 20 (40 μL) 200 μL
LYRM4-FARS2-20-GOAQ 20 (40 μL) 200 μL
LYRM4-FARS2-20-GRRE 20 (40 μL) 200 μL
LYRM4-FARS2-20-GROR 20 (40 μL) 200 μL
LYRM4-FARS2-20-GRGO 20 (40 μL) 200 μL
LYRM4-FARS2-20-GRGR 20 (40 μL) 200 μL
LYRM4-FARS2-20-GRAQ 20 (40 μL) 200 μL
LYRM4-FARS2-20-AQRE 20 (40 μL) 200 μL
LYRM4-FARS2-20-AQOR 20 (40 μL) 200 μL
LYRM4-FARS2-20-AQGO 20 (40 μL) 200 μL
LYRM4-FARS2-20-AQGR 20 (40 μL) 200 μL
LYRM4-FARS2-20-AQAQ 20 (40 μL) 200 μL

FARS2 Gene Summary

This gene encodes a protein that transfers phenylalanine to its cognate tRNA. This protein localizes to the mitochondrion and plays a role in mitochondrial protein translation. Mutations in this gene can cause combined oxidative phosphorylation deficiency 14 (Alpers encephalopathy). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]

Gene Name: Phenylalanyl-tRNA Synthetase 2, Mitochondrial

Chromosome: CHR6: 5261583 -5771816

Locus: 6p25.1

LYRM4 Gene Summary

The protein encoded by this gene is found in both mitochondria and the nucleus, where it binds cysteine desulfurase and helps free inorganic sulfur for Fe/S clusters. Disruption of this gene negatively impacts mitochondrial and cytosolic iron homeostasis. [provided by RefSeq, Sep 2016]

Gene Name: LYR Motif Containing 4

Chromosome: CHR6: 5108652 -5261172

Locus: 6p25.1

Gene Diseases

The LYRM4 FARS2 Fusion has been associated with the following diseases:

Disease Name
Skin Cutaneous Melanoma
Cervical Squamous Cell Carcinoma And Endocervical Adenocarcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.