人 SSX2B (NM_001278702) cDNA克隆

Accession: NM_001278702
基因名称: SSX2B
基因别名: SSX; CT5.2; CT5.2b; HOM-MEL-40
基因描述: Homo sapiens synovial sarcoma, X breakpoint 2B (SSX2B), transcript variant 3, mRNA.
种属: Human
CDS区长度: 645 (查看编码区序列)
翻译后氨基酸长度: 214 (查看氨基酸序列)
Transcript Variant: This variant (3) uses an alternate splice site that results in a frameshift in the 3' coding region, compared to variant 1. The encoded isoform (c) contains a shorter and distinct C-terminus, compared to isoform a.
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G163009 人 SSX2B (NM_001278702) cDNA克隆 pDONR223 2ug质粒 点击询价

The product of this gene belongs to the family of highly homologous synovial sarcoma X (SSX) breakpoint proteins. These proteins may function as transcriptional repressors. They are also capable of eliciting spontaneous humoral and cellular immune responses in cancer patients, and are potentially useful targets in cancer vaccine-based immunotherapy. This gene, and also the SSX1 and SSX4 family members, have been involved in t(X;18)(p11.2;q11.2) translocations that are characteristically found in all synovial sarcomas. This translocation results in the fusion of the synovial sarcoma translocation gene on chromosome 18 to one of the SSX genes on chromosome X. The encoded hybrid proteins are likely responsible for transforming activity. Alternative splicing of this gene results in multiple transcript variants. This gene also has an identical duplicate, GeneID: 6757, located about 45 kb upstream in the opposite orientation on chromosome X. [provided by RefSeq, Jul 2013]