Description
excision repair cross-complementing rodent repair deficiency, complementation group 2 [Source:HGNC Symbol;Acc:3434]
Location
Chromosome 19: 45,854,246-45,873,876 reverse strand.
Transcripts
This gene has 7 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
ERCC2-001ENST000003919453002ENSP00000375809760Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS33049
ERCC2-002ENST000003919422982ENSP00000375806736Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
ERCC2-003ENST000003919413137ENSP00000375805710Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
ERCC2-201ENST00000221481745ENSP00000221481127Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
ERCC2-202ENST000003919401300ENSP00000375804405Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS46112
ERCC2-203ENST000003919442103ENSP00000375808682Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
ERCC2-004ENST000004854032918ENSP00000431229470Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -

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.