DGCR2-SLC25A1 Fusion FISH Probe
The DGCR2-SLC25A1 Fusion FISH Probe is used to confirm a fusion of the DGCR2 and SLC25A1 genes. The fusion of the DGCR2 and SLC25A1 genes has been associated with Stomach 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| DGCR2-SLC25A1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| DGCR2-SLC25A1-20-RERE | 20 (40 μL) | 200 μL |
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| DGCR2-SLC25A1-20-REOR | 20 (40 μL) | 200 μL |
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| DGCR2-SLC25A1-20-REGO | 20 (40 μL) | 200 μL |
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| DGCR2-SLC25A1-20-REGR | 20 (40 μL) | 200 μL |
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| DGCR2-SLC25A1-20-REAQ | 20 (40 μL) | 200 μL |
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| DGCR2-SLC25A1-20-ORRE | 20 (40 μL) | 200 μL |
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| DGCR2-SLC25A1-20-OROR | 20 (40 μL) | 200 μL |
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| DGCR2-SLC25A1-20-ORGO | 20 (40 μL) | 200 μL |
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| DGCR2-SLC25A1-20-ORAQ | 20 (40 μL) | 200 μL |
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| DGCR2-SLC25A1-20-GORE | 20 (40 μL) | 200 μL |
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| DGCR2-SLC25A1-20-GOOR | 20 (40 μL) | 200 μL |
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| DGCR2-SLC25A1-20-GOGO | 20 (40 μL) | 200 μL |
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| DGCR2-SLC25A1-20-GOGR | 20 (40 μL) | 200 μL |
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| DGCR2-SLC25A1-20-GOAQ | 20 (40 μL) | 200 μL |
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| DGCR2-SLC25A1-20-GRRE | 20 (40 μL) | 200 μL |
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| DGCR2-SLC25A1-20-GROR | 20 (40 μL) | 200 μL |
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| DGCR2-SLC25A1-20-GRGO | 20 (40 μL) | 200 μL |
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| DGCR2-SLC25A1-20-GRGR | 20 (40 μL) | 200 μL |
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| DGCR2-SLC25A1-20-GRAQ | 20 (40 μL) | 200 μL |
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| DGCR2-SLC25A1-20-AQRE | 20 (40 μL) | 200 μL |
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| DGCR2-SLC25A1-20-AQOR | 20 (40 μL) | 200 μL |
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| DGCR2-SLC25A1-20-AQGO | 20 (40 μL) | 200 μL |
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| DGCR2-SLC25A1-20-AQGR | 20 (40 μL) | 200 μL |
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| DGCR2-SLC25A1-20-AQAQ | 20 (40 μL) | 200 μL |
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SLC25A1 Gene Summary
This gene encodes a member of the mitochondrial carrier subfamily of solute carrier proteins. Members of this family include nuclear-encoded transporters that translocate small metabolites across the mitochondrial membrane. This protein regulates the movement of citrate across the inner membranes of the mitochondria. Mutations in this gene have been associated with combined D-2- and L-2-hydroxyglutaric aciduria. Pseudogenes of this gene have been identified on chromosomes 7, 11, 16, and 19. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]
Gene Name: Solute Carrier Family 25 Member 1
Chromosome: CHR22: 19163093 -19166301
Locus: 22q11.21
DGCR2 Gene Summary
Deletions of the 22q11.2 have been associated with a wide range of developmental defects (notably DiGeorge syndrome, velocardiofacial syndrome, conotruncal anomaly face syndrome and isolated conotruncal cardiac defects) classified under the acronym CATCH 22. The DGCR2 gene encodes a novel putative adhesion receptor protein, which could play a role in neural crest cells migration, a process which has been proposed to be altered in DiGeorge syndrome. Alternative splicing results in multiple transcript variants.[provided by RefSeq, May 2010]
Gene Name: DiGeorge Syndrome Critical Region Gene 2
Chromosome: CHR22: 19023794 -19109967
Locus: 22q11.21
Gene Diseases
The DGCR2 SLC25A1 Fusion has been associated with the following diseases:
| Disease Name |
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| Stomach Adenocarcinoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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