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FANCD2-MTMR14 Fusion FISH Probe

The FANCD2-MTMR14 Fusion FISH Probe is used to confirm a fusion of the FANCD2 and MTMR14 genes. The fusion of the FANCD2 and MTMR14 genes has been associated with Stomach Adenocarcinoma, and Breast Invasive 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.

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

SKU Test Kits Buffer Dye Color Order Now
FANCD2-MTMR14-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
FANCD2-MTMR14-20-RERE 20 (40 μL) 200 μL
FANCD2-MTMR14-20-REOR 20 (40 μL) 200 μL
FANCD2-MTMR14-20-REGO 20 (40 μL) 200 μL
FANCD2-MTMR14-20-REGR 20 (40 μL) 200 μL
FANCD2-MTMR14-20-REAQ 20 (40 μL) 200 μL
FANCD2-MTMR14-20-ORRE 20 (40 μL) 200 μL
FANCD2-MTMR14-20-OROR 20 (40 μL) 200 μL
FANCD2-MTMR14-20-ORGO 20 (40 μL) 200 μL
FANCD2-MTMR14-20-ORAQ 20 (40 μL) 200 μL
FANCD2-MTMR14-20-GORE 20 (40 μL) 200 μL
FANCD2-MTMR14-20-GOOR 20 (40 μL) 200 μL
FANCD2-MTMR14-20-GOGO 20 (40 μL) 200 μL
FANCD2-MTMR14-20-GOGR 20 (40 μL) 200 μL
FANCD2-MTMR14-20-GOAQ 20 (40 μL) 200 μL
FANCD2-MTMR14-20-GRRE 20 (40 μL) 200 μL
FANCD2-MTMR14-20-GROR 20 (40 μL) 200 μL
FANCD2-MTMR14-20-GRGO 20 (40 μL) 200 μL
FANCD2-MTMR14-20-GRGR 20 (40 μL) 200 μL
FANCD2-MTMR14-20-GRAQ 20 (40 μL) 200 μL
FANCD2-MTMR14-20-AQRE 20 (40 μL) 200 μL
FANCD2-MTMR14-20-AQOR 20 (40 μL) 200 μL
FANCD2-MTMR14-20-AQGO 20 (40 μL) 200 μL
FANCD2-MTMR14-20-AQGR 20 (40 μL) 200 μL
FANCD2-MTMR14-20-AQAQ 20 (40 μL) 200 μL

FANCD2 Gene Summary

The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group D2. This protein is monoubiquinated in response to DNA damage, resulting in its localization to nuclear foci with other proteins (BRCA1 AND BRCA2) involved in homology-directed DNA repair. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]

Gene Name: Fanconi Anemia Complementation Group D2

Chromosome: CHR3: 10068112 -10143614

Locus: 3p25.3

MTMR14 Gene Summary

This gene encodes a myotubularin-related protein. The encoded protein is a phosphoinositide phosphatase that specifically dephosphorylates phosphatidylinositol 3,5-biphosphate and phosphatidylinositol 3-phosphate. Mutations in this gene are correlated with autosomal dominant centronuclear myopathy. Alternate splicing results in multiple transcript variants. A pseudogene of this gene is found on chromosome 18.[provided by RefSeq, Apr 2010]

Gene Name: Myotubularin Related Protein 14

Chromosome: CHR3: 9691116 -9744078

Locus: 3p25.3

Gene Diseases

The FANCD2 MTMR14 Fusion has been associated with the following diseases:

Disease Name
Stomach Adenocarcinoma
Breast Invasive Carcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.