Homo sapiens Gene: SSX1 | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Gene | IDBG-62613.6 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | SSX1 | ||||||||||||||||||
Gene Name | synovial sarcoma, X breakpoint 1 | ||||||||||||||||||
Synonyms | CT5.1; SSRC | ||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Gene | ENSG00000126752 | ||||||||||||||||||
Encoded Proteins |
synovial sarcoma, X breakpoint 1
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Protein Structure |
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Useful resources | Stemformatics EHFPI ImmGen | ||||||||||||||||||
Entrez Gene | |||||||||||||||||||
Summary |
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 spontaneously humoral and cellular immune responses in cancer patients, and are potentially useful targets in cancer vaccine-based immunotherapy. SSX1, SSX2 and SSX4 genes have been involved in the t(X;18) translocation 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 probably responsible for transforming activity. [provided by RefSeq, Jul 2008] 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 SSX2 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. A related pseudogene has been identified on chromosome X. [provided by RefSeq, Jul 2013] |
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Gene Information | |||||||||||||||||||
Type | Protein coding | ||||||||||||||||||
Genomic Location | Chromosome X:48255317-48267444 | ||||||||||||||||||
Strand | Forward strand | ||||||||||||||||||
Band | p11.23 | ||||||||||||||||||
Transcripts |
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Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 4 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Orthologs | |||||||||||||||||||
No orthologs found for this gene | |||||||||||||||||||
Cross-References | |||||||||||||||||||
SwissProt | Q16384 | ||||||||||||||||||
TrEMBL | |||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 6756 | ||||||||||||||||||
UniGene | Hs.434142 | ||||||||||||||||||
RefSeq | NM_001278691 NM_005635 | ||||||||||||||||||
HUGO | HGNC:11335 | ||||||||||||||||||
OMIM | 312820 | ||||||||||||||||||
CCDS | CCDS14290 | ||||||||||||||||||
HPRD | |||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AL683817 BC001003 BC125151 BC128611 BC133693 BC150487 S79325 X86174 | ||||||||||||||||||
GenPept | AAB35378 AAH01003 AAI25152 AAI28612 AAI33694 AAI50488 CAA60110 CAI41141 | ||||||||||||||||||
RNA Seq Atlas | 6756 | ||||||||||||||||||