GNAS-SNW1 Fusion FISH Probe
The GNAS-SNW1 Fusion FISH Probe is used to confirm a fusion of the GNAS and SNW1 genes. The fusion of the GNAS and SNW1 genes has been associated with 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.
SKU | Test Kits | Buffer | Dye Color | Order Now |
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GNAS-SNW1-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
GNAS-SNW1-20-RERE | 20 (40 μL) | 200 μL | ||
GNAS-SNW1-20-REOR | 20 (40 μL) | 200 μL | ||
GNAS-SNW1-20-REGO | 20 (40 μL) | 200 μL | ||
GNAS-SNW1-20-REGR | 20 (40 μL) | 200 μL | ||
GNAS-SNW1-20-REAQ | 20 (40 μL) | 200 μL | ||
GNAS-SNW1-20-ORRE | 20 (40 μL) | 200 μL | ||
GNAS-SNW1-20-OROR | 20 (40 μL) | 200 μL | ||
GNAS-SNW1-20-ORGO | 20 (40 μL) | 200 μL | ||
GNAS-SNW1-20-ORAQ | 20 (40 μL) | 200 μL | ||
GNAS-SNW1-20-GORE | 20 (40 μL) | 200 μL | ||
GNAS-SNW1-20-GOOR | 20 (40 μL) | 200 μL | ||
GNAS-SNW1-20-GOGO | 20 (40 μL) | 200 μL | ||
GNAS-SNW1-20-GOGR | 20 (40 μL) | 200 μL | ||
GNAS-SNW1-20-GOAQ | 20 (40 μL) | 200 μL | ||
GNAS-SNW1-20-GRRE | 20 (40 μL) | 200 μL | ||
GNAS-SNW1-20-GROR | 20 (40 μL) | 200 μL | ||
GNAS-SNW1-20-GRGO | 20 (40 μL) | 200 μL | ||
GNAS-SNW1-20-GRGR | 20 (40 μL) | 200 μL | ||
GNAS-SNW1-20-GRAQ | 20 (40 μL) | 200 μL | ||
GNAS-SNW1-20-AQRE | 20 (40 μL) | 200 μL | ||
GNAS-SNW1-20-AQOR | 20 (40 μL) | 200 μL | ||
GNAS-SNW1-20-AQGO | 20 (40 μL) | 200 μL | ||
GNAS-SNW1-20-AQGR | 20 (40 μL) | 200 μL | ||
GNAS-SNW1-20-AQAQ | 20 (40 μL) | 200 μL |
GNAS Gene Summary
This locus has a highly complex imprinted expression pattern. It gives rise to maternally, paternally, and biallelically expressed transcripts that are derived from four alternative promoters and 5' exons. Some transcripts contain a differentially methylated region (DMR) at their 5' exons, and this DMR is commonly found in imprinted genes and correlates with transcript expression. An antisense transcript is produced from an overlapping locus on the opposite strand. One of the transcripts produced from this locus, and the antisense transcript, are paternally expressed noncoding RNAs, and may regulate imprinting in this region. In addition, one of the transcripts contains a second overlapping ORF, which encodes a structurally unrelated protein - Alex. Alternative splicing of downstream exons is also observed, which results in different forms of the stimulatory G-protein alpha subunit, a key element of the classical signal transduction pathway linking receptor-ligand interactions with the activation of adenylyl cyclase and a variety of cellular reponses. Multiple transcript variants encoding different isoforms have been found for this gene. Mutations in this gene result in pseudohypoparathyroidism type 1a, pseudohypoparathyroidism type 1b, Albright hereditary osteodystrophy, pseudopseudohypoparathyroidism, McCune-Albright syndrome, progressive osseus heteroplasia, polyostotic fibrous dysplasia of bone, and some pituitary tumors. [provided by RefSeq, Aug 2012]
Gene Name: GNAS Complex Locus
Chromosome: CHR20: 57414794 -57486250
Locus: 20q13.32
SNW1 Gene Summary
This gene, a member of the SNW gene family, encodes a coactivator that enhances transcription from some Pol II promoters. This coactivator can bind to the ligand-binding domain of the vitamin D receptor and to retinoid receptors to enhance vitamin D-, retinoic acid-, estrogen-, and glucocorticoid-mediated gene expression. It can also function as a splicing factor by interacting with poly(A)-binding protein 2 to directly control the expression of muscle-specific genes at the transcriptional level. Finally, the protein may be involved in oncogenesis since it interacts with a region of SKI oncoproteins that is required for transforming activity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]
Gene Name: SNW Domain Containing 1
Chromosome: CHR14: 78183943 -78227497
Locus: 14q24.3
Gene Diseases
The GNAS SNW1 Fusion has been associated with the following diseases:
Disease Name |
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Cervical Squamous Cell Carcinoma And Endocervical Adenocarcinoma |
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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