Description
chromosome 22 open reading frame 13 [Source:HGNC Symbol;Acc:14237]
Location
Chromosome 22: 24,936,406-24,951,903 reverse strand.
Transcripts
This gene has 12 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
C22orf13-001ENST000004074713482ENSP00000386076240Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS33621
C22orf13-002ENST000004358223613ENSP00000405985239Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
C22orf13-003ENST000004046641606ENSP00000384121295Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
C22orf13-005ENST00000407973773ENSP00000385583127Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
C22orf13-008ENST00000402766865ENSP00000384378137Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
C22orf13-009ENST00000447813895ENSP00000387867136Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
C22orf13-004ENST000003982451593ENSP00000381297239Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
C22orf13-010ENST00000490922567No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
C22orf13-011ENST00000490810346No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
C22orf13-012ENST00000493099510No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
C22orf13-006ENST00000468170619No protein product-Retained intronNoncoding transcript containing intronic sequence. -
C22orf13-007ENST00000480272516No 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.