Human Gene SSX5 (uc004diz.1)
  Description: Homo sapiens synovial sarcoma, X breakpoint 5 (SSX5), transcript variant 1, mRNA.
RefSeq Summary (NM_021015): 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. While some of the related SSX genes are involved in t(X;18)(p11.2;q11.2) translocations that are characteristically found in all synovial sarcomas, this gene does not appear to be involved in such translocations. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2013].
Transcript (Including UTRs)
   Position: hg19 chrX:48,045,656-48,056,199 Size: 10,544 Total Exon Count: 9 Strand: -
Coding Region
   Position: hg19 chrX:48,047,067-48,054,794 Size: 7,728 Coding Exon Count: 7 

Page IndexSequence and LinksPrimersMalaCardsCTDGene Alleles
RNA-Seq ExpressionMicroarray ExpressionRNA StructureProtein StructureOther SpeciesmRNA Descriptions
Other NamesModel InformationMethods
Data last updated at UCSC: 2013-06-14

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chrX:48,045,656-48,056,199)mRNA (may differ from genome)Protein (229 aa)
Gene SorterGenome BrowserOther Species FASTAGene interactionsTable SchemaAlphaFold
BioGPSEnsemblEntrez GeneExonPrimerGeneCardsGeneNetwork
H-INVHGNCHPRDLynxMalacardsMGI
OMIMPubMedTreefamUniProtKBWikipediaBioGrid CRISPR DB

-  Primer design for this transcript
 

Primer3Plus can design qPCR Primers that straddle exon-exon-junctions, which amplify only cDNA, not genomic DNA.
Click here to load the transcript sequence and exon structure into Primer3Plus

Exonprimer can design one pair of Sanger sequencing primers around every exon, located in non-genic sequence.
Click here to open Exonprimer with this transcript

To design primers for a non-coding sequence, zoom to a region of interest and select from the drop-down menu: View > In External Tools > Primer3


-  MalaCards Disease Associations
  MalaCards Gene Search: SSX5
Diseases sorted by gene-association score: sarcoma (11), synovium cancer (2)

-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene

+  Common Gene Haplotype Alleles
  Press "+" in the title bar above to open this section.

-  RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
  Highest median expression: 0.58 RPKM in Testis
Total median expression: 0.62 RPKM



View in GTEx track of Genome Browser    View at GTEx portal     View GTEx Body Map

+  Microarray Expression Data
  Press "+" in the title bar above to open this section.

-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -11.8053-0.223 Picture PostScript Text
3' UTR -151.39641-0.236 Picture PostScript Text

The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.

-  Protein Domain and Structure Information
  Pfam Domains:
PF09514 - SSXRD motif

SCOP Domains:
109640 - KRAB domain (Kruppel-associated box, Pfam 01352)

ModBase Predicted Comparative 3D Structure on O60225-2
FrontTopSide
The pictures above may be empty if there is no ModBase structure for the protein. The ModBase structure frequently covers just a fragment of the protein. You may be asked to log onto ModBase the first time you click on the pictures. It is simplest after logging in to just click on the picture again to get to the specific info on that model.

-  Orthologous Genes in Other Species
  Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
MouseRatZebrafishD. melanogasterC. elegansS. cerevisiae
No orthologNo orthologNo orthologNo orthologNo orthologNo ortholog
      
      
      
      
      

-  Descriptions from all associated GenBank mRNAs
  BC016640 - Homo sapiens synovial sarcoma, X breakpoint 5, mRNA (cDNA clone MGC:9494 IMAGE:3923927), complete cds.
JD188073 - Sequence 169097 from Patent EP1572962.
JD097136 - Sequence 78160 from Patent EP1572962.
JD163522 - Sequence 144546 from Patent EP1572962.
JD411576 - Sequence 392600 from Patent EP1572962.
JD039261 - Sequence 20285 from Patent EP1572962.
JD267802 - Sequence 248826 from Patent EP1572962.
JD090320 - Sequence 71344 from Patent EP1572962.
JD152494 - Sequence 133518 from Patent EP1572962.
JD390678 - Sequence 371702 from Patent EP1572962.
AX740219 - Sequence 2 from Patent EP1300463.
U90842 - Homo sapiens SSX5 (SSX5) mRNA, complete cds.
HQ258017 - Synthetic construct Homo sapiens clone IMAGE:100072326 synovial sarcoma, X breakpoint 5 (SSX5) gene, encodes complete protein.
KJ897608 - Synthetic construct Homo sapiens clone ccsbBroadEn_07002 SSX5 gene, encodes complete protein.
EU446708 - Synthetic construct Homo sapiens clone IMAGE:100070050; IMAGE:100011917; FLH258268.01L synovial sarcoma, X breakpoint 5 (SSX5) gene, encodes complete protein.
AB527939 - Synthetic construct DNA, clone: pF1KB0977, Homo sapiens SSX5 gene for Protein SSX5, without stop codon, in Flexi system.
JD126038 - Sequence 107062 from Patent EP1572962.
JD126037 - Sequence 107061 from Patent EP1572962.
JD289109 - Sequence 270133 from Patent EP1572962.

-  Other Names for This Gene
  Alternate Gene Symbols: NM_021015, NP_066295, O60225-2
UCSC ID: uc004diz.1
RefSeq Accession: NM_021015
Protein: O60225-2, splice isoform of O60225 CCDS: CCDS14288.1

-  Gene Model Information
 
category: coding nonsense-mediated-decay: no RNA accession: NM_021015.3
exon count: 9CDS single in 3' UTR: no RNA size: 1399
ORF size: 690CDS single in intron: no Alignment % ID: 100.00
txCdsPredict score: 1340.00frame shift in genome: no % Coverage: 98.93
has start codon: yes stop codon in genome: no # of Alignments: 1
has end codon: yes retained intron: no # AT/AC introns 0
selenocysteine: no end bleed into intron: 0# strange splices: 0
Click here for a detailed description of the fields of the table above.

-  Methods, Credits, and Use Restrictions
  Click here for details on how this gene model was made and data restrictions if any.