Description
Sjogren syndrome antigen B (autoantigen La) [Source:HGNC Symbol;Acc:11316]
Location
Chromosome 2: 170,648,443-170,668,574 forward strand.
Transcripts
This gene has 14 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
SSB-001ENST000002609561709ENSP00000260956408Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS2237
SSB-002ENST000004090051457ENSP00000386524361Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
SSB-003ENST000004093331782ENSP00000386636408Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS2237
SSB-004ENST000004220062463ENSP00000397029184Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
SSB-005ENST00000417292545ENSP00000396890120Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
SSB-201ENST00000544688672ENSP0000043785183Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
SSB-006ENST00000413002674ENSP00000395758134Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
SSB-007ENST00000461708619No protein product-Retained intronNoncoding transcript containing intronic sequence. -
SSB-008ENST00000468600290No protein product-Retained intronNoncoding transcript containing intronic sequence. -
SSB-009ENST00000474273735No protein product-Retained intronNoncoding transcript containing intronic sequence. -
SSB-010ENST00000465871421No protein product-Retained intronNoncoding transcript containing intronic sequence. -
SSB-011ENST00000490914754No protein product-Retained intronNoncoding transcript containing intronic sequence. -
SSB-012ENST00000494051392No protein product-Retained intronNoncoding transcript containing intronic sequence. -
SSB-013ENST00000470621440No protein product-Retained intronNoncoding transcript containing intronic sequence. -

Transcript and Gene level displays

In Archive EnsEMBL we provide displays at two levels:

  • Transcript views which provide information specific to an individual transcript such as the cDNA and CDS sequences and protein domain annotation.
  • Gene views which provide displays for data associated at the gene level such as orthologues, paralogues, regulatory regions and splice variants.

This view is a gene level view. To access the transcript level displays select a Transcript ID in the table above and then navigate to the information you want using the menu at the left hand side of the page. To return to viewing gene level information click on the Gene tab in the menu bar at the top of the page.