Description
autoimmune regulator [Source:HGNC Symbol;Acc:360]
Location
Chromosome 21: 45,705,721-45,718,531 forward strand.
Transcripts
This gene has 8 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
AIRE-001ENST000002915822257ENSP00000291582545Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS13706
AIRE-002ENST000003379091542ENSP00000337986348Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS13707
AIRE-201ENST000003293471427ENSP00000331055244Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
AIRE-202ENST000003553471509ENSP00000347505338Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
AIRE-203ENST000003979941963ENSP00000381080348Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS13707
AIRE-003ENST000004682821460ENSP00000435713254Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
AIRE-004ENST000005279192409No protein product-Retained intronNoncoding transcript containing intronic sequence. -
AIRE-005ENST000005308124306No 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.