Our SS18 break apart probe is designed to detect SS18 translocations. The probe comes labeled in green and orange, but can be customized to meet your needs. 

Gene Background: SS18 is frequently rearranged in synovial sarcoma, an aggressive neoplasm accounting for 10-20% of soft tissue sarcomas in the adolescent and young adult population. Approximately 70% of cases present in the extremities, with a tendency to metastasize to the lungs. The balanced chromosomal translocation t(X,18; p11,q11) is present in virtually all cases of synovial sarcoma. The rearrangement creates an in-frame fusion of the SS18 gene to SSX1 or SSX2, whereby all but the C-terminal eight amino acids of SS18 become fused to the C-terminal 78 amino acids of the SS18 partner. An analogous translocation of SSX4 is present in less than 1% of cases. SS18-SSX fusion is the sole cytogenetic abnormality in up to a third of synovial sarcomas, and is now considered a central driver of the disease.

Source: Nielsen T, et al. (2015) Cancer discovery 5.2: 124-134.

** This product is for in vitro and research use only. This product is not intended for diagnostic use.

Gene Summary

The SS18, NBAF Chromatin Remodeling Complex Subunit (SS18) gene is located on chr18:23596216 -23670611 at 18q11.2.

Gene Details

Gene Symbol: SS18

Gene Name: SS18, NBAF Chromatin Remodeling Complex Subunit

Chromosome: CHR18: 23596216-23670611

Locus: 18q11.2

References

Customer Publications

There are currently no FISH related publications for this gene.