ATRX-SNTB2 Fusion FISH Probe
The ATRX-SNTB2 Fusion FISH Probe is used to confirm a fusion of the ATRX and SNTB2 genes. The fusion of the ATRX and SNTB2 genes has been associated with Sarcoma. 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.
| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| ATRX-SNTB2-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| ATRX-SNTB2-20-RERE | 20 (40 μL) | 200 μL |
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| ATRX-SNTB2-20-REOR | 20 (40 μL) | 200 μL |
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| ATRX-SNTB2-20-REGO | 20 (40 μL) | 200 μL |
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| ATRX-SNTB2-20-REGR | 20 (40 μL) | 200 μL |
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| ATRX-SNTB2-20-REAQ | 20 (40 μL) | 200 μL |
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| ATRX-SNTB2-20-ORRE | 20 (40 μL) | 200 μL |
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| ATRX-SNTB2-20-OROR | 20 (40 μL) | 200 μL |
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| ATRX-SNTB2-20-ORGO | 20 (40 μL) | 200 μL |
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| ATRX-SNTB2-20-ORAQ | 20 (40 μL) | 200 μL |
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| ATRX-SNTB2-20-GORE | 20 (40 μL) | 200 μL |
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| ATRX-SNTB2-20-GOOR | 20 (40 μL) | 200 μL |
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| ATRX-SNTB2-20-GOGO | 20 (40 μL) | 200 μL |
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| ATRX-SNTB2-20-GOGR | 20 (40 μL) | 200 μL |
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| ATRX-SNTB2-20-GOAQ | 20 (40 μL) | 200 μL |
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| ATRX-SNTB2-20-GRRE | 20 (40 μL) | 200 μL |
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| ATRX-SNTB2-20-GROR | 20 (40 μL) | 200 μL |
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| ATRX-SNTB2-20-GRGO | 20 (40 μL) | 200 μL |
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| ATRX-SNTB2-20-GRGR | 20 (40 μL) | 200 μL |
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| ATRX-SNTB2-20-GRAQ | 20 (40 μL) | 200 μL |
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| ATRX-SNTB2-20-AQRE | 20 (40 μL) | 200 μL |
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| ATRX-SNTB2-20-AQOR | 20 (40 μL) | 200 μL |
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| ATRX-SNTB2-20-AQGO | 20 (40 μL) | 200 μL |
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| ATRX-SNTB2-20-AQGR | 20 (40 μL) | 200 μL |
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| ATRX-SNTB2-20-AQAQ | 20 (40 μL) | 200 μL |
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ATRX Gene Summary
The protein encoded by this gene contains an ATPase/helicase domain, and thus it belongs to the SWI/SNF family of chromatin remodeling proteins. This protein is found to undergo cell cycle-dependent phosphorylation, which regulates its nuclear matrix and chromatin association, and suggests its involvement in the gene regulation at interphase and chromosomal segregation in mitosis. Mutations in this gene are associated with X-linked syndromes exhibiting cognitive disabilities as well as alpha-thalassemia (ATRX) syndrome. These mutations have been shown to cause diverse changes in the pattern of DNA methylation, which may provide a link between chromatin remodeling, DNA methylation, and gene expression in developmental processes. Multiple alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2017]
Gene Name: ATRX, Chromatin Remodeler
Chromosome: CHRX: 76760355 -77041719
Locus: Xq21.1
SNTB2 Gene Summary
Dystrophin is a large, rod-like cytoskeletal protein found at the inner surface of muscle fibers. Dystrophin is missing in Duchenne Muscular Dystrophy patients and is present in reduced amounts in Becker Muscular Dystrophy patients. The protein encoded by this gene is a peripheral membrane protein found associated with dystrophin and dystrophin-related proteins. This gene is a member of the syntrophin gene family, which contains at least two other structurally-related genes. [provided by RefSeq, Jul 2008]
Gene Name: Syntrophin Beta 2
Chromosome: CHR16: 69221049 -69342955
Locus: 16q22.1
Gene Diseases
The ATRX SNTB2 Fusion has been associated with the following diseases:
| Disease Name |
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| Sarcoma |
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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