Description
interferon regulatory factor 2 [Source:HGNC Symbol;Acc:6117]
Location
Chromosome 4: 185,308,867-185,395,734 reverse strand.
Transcripts
This gene has 10 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
IRF2-001ENST000003935932303ENSP00000377218349Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS3835
IRF2-002ENST00000505316665ENSP00000423506137Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
IRF2-004ENST00000506230498ENSP00000422860137Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
IRF2-005ENST00000507523595ENSP00000427204176Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
IRF2-007ENST00000510814568ENSP00000424552161Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
IRF2-009ENST00000505067586ENSP00000421927196Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
IRF2-010ENST00000502750339ENSP00000423074113Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
IRF2-006ENST00000509274591ENSP0000042503783Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
IRF2-008ENST00000512020731ENSP00000424475129Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
IRF2-003ENST00000504340565No 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.