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SMARCAD1-GRID2 Fusion FISH Probe

The SMARCAD1-GRID2 Fusion FISH Probe is used to confirm a fusion of the SMARCAD1 and GRID2 genes. The fusion of the SMARCAD1 and GRID2 genes has been associated with Brain Lower Grade Glioma. 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
SMARCAD1-GRID2-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
SMARCAD1-GRID2-20-RERE 20 (40 μL) 200 μL
SMARCAD1-GRID2-20-REOR 20 (40 μL) 200 μL
SMARCAD1-GRID2-20-REGO 20 (40 μL) 200 μL
SMARCAD1-GRID2-20-REGR 20 (40 μL) 200 μL
SMARCAD1-GRID2-20-REAQ 20 (40 μL) 200 μL
SMARCAD1-GRID2-20-ORRE 20 (40 μL) 200 μL
SMARCAD1-GRID2-20-OROR 20 (40 μL) 200 μL
SMARCAD1-GRID2-20-ORGO 20 (40 μL) 200 μL
SMARCAD1-GRID2-20-ORAQ 20 (40 μL) 200 μL
SMARCAD1-GRID2-20-GORE 20 (40 μL) 200 μL
SMARCAD1-GRID2-20-GOOR 20 (40 μL) 200 μL
SMARCAD1-GRID2-20-GOGO 20 (40 μL) 200 μL
SMARCAD1-GRID2-20-GOGR 20 (40 μL) 200 μL
SMARCAD1-GRID2-20-GOAQ 20 (40 μL) 200 μL
SMARCAD1-GRID2-20-GRRE 20 (40 μL) 200 μL
SMARCAD1-GRID2-20-GROR 20 (40 μL) 200 μL
SMARCAD1-GRID2-20-GRGO 20 (40 μL) 200 μL
SMARCAD1-GRID2-20-GRGR 20 (40 μL) 200 μL
SMARCAD1-GRID2-20-GRAQ 20 (40 μL) 200 μL
SMARCAD1-GRID2-20-AQRE 20 (40 μL) 200 μL
SMARCAD1-GRID2-20-AQOR 20 (40 μL) 200 μL
SMARCAD1-GRID2-20-AQGO 20 (40 μL) 200 μL
SMARCAD1-GRID2-20-AQGR 20 (40 μL) 200 μL
SMARCAD1-GRID2-20-AQAQ 20 (40 μL) 200 μL

GRID2 Gene Summary

The protein encoded by this gene is a member of the family of ionotropic glutamate receptors which are the predominant excitatory neurotransmitter receptors in the mammalian brain. The encoded protein is a multi-pass membrane protein that is expressed selectively in cerebellar Purkinje cells. A point mutation in the mouse ortholog, associated with the phenotype named 'lurcher', in the heterozygous state leads to ataxia resulting from selective, cell-autonomous apoptosis of cerebellar Purkinje cells during postnatal development. Mice homozygous for this mutation die shortly after birth from massive loss of mid- and hindbrain neurons during late embryogenesis. This protein also plays a role in synapse organization between parallel fibers and Purkinje cells. Alternate splicing results in multiple transcript variants encoding distinct isoforms. Mutations in this gene cause cerebellar ataxia in humans. [provided by RefSeq, Apr 2014]

Gene Name: Glutamate Ionotropic Receptor Delta Type Subunit 2

Chromosome: CHR4: 93225549 -94693649

Locus: 4q22.1-q22.2

SMARCAD1 Gene Summary

This gene encodes a member of the SNF subfamily of helicase proteins. The encoded protein plays a critical role in the restoration of heterochromatin organization and propagation of epigenetic patterns following DNA replication by mediating histone H3/H4 deacetylation. Mutations in this gene are associated with adermatoglyphia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]

Gene Name: SWI/SNF-related, Matrix-associated Actin-dependent Regulator Of Chromatin, Subfamily A, Containing DEAD/H Box 1

Chromosome: CHR4: 95128758 -95212443

Locus: 4q22.3

Gene Diseases

The SMARCAD1 GRID2 Fusion has been associated with the following diseases:

Disease Name
Brain Lower Grade Glioma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.