Description
interferon (alpha, beta and omega) receptor 2 [Source:HGNC Symbol;Acc:5433]
Location
Chromosome 21: 34,602,206-34,637,969 forward strand.
Transcripts
This gene has 11 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
IFNAR2-001ENST000004042204335ENSP00000384309331Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS13622
IFNAR2-002ENST000003421362899ENSP00000343957515Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS13621
IFNAR2-003ENST000003421012606ENSP00000343289239Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
IFNAR2-004ENST000003822641389ENSP00000371699331Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS13622
IFNAR2-008ENST00000447980726ENSP00000402311204Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
IFNAR2-009ENST00000413881710ENSP00000413160167Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
IFNAR2-010ENST00000443073841ENSP00000403569229Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
IFNAR2-201ENST000003822412889ENSP00000371676515Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS13621
IFNAR2-006ENST000003822381127ENSP00000371673197Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
IFNAR2-007ENST00000417007719ENSP0000039879954Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
IFNAR2-020ENST00000420068505No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -

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.