Description
ADAM metallopeptidase domain 8 [Source:HGNC Symbol;Acc:215]
Location
Chromosome 10: 135,075,907-135,090,372 reverse strand.
Transcripts
This gene has 11 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
ADAM8-001ENST000004453553279ENSP00000453302824Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
ADAM8-004ENST00000486609776ENSP00000453735245Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
ADAM8-005ENST000004854912441ENSP00000453043733Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
ADAM8-009ENST000004152173077ENSP00000453855742Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
ADAM8-007ENST00000560135818ENSP00000452994109Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
ADAM8-006ENST00000559180560No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
ADAM8-002ENST00000468964613No protein product-Retained intronNoncoding transcript containing intronic sequence. -
ADAM8-003ENST000004632981122No protein product-Retained intronNoncoding transcript containing intronic sequence. -
ADAM8-008ENST000005370991579No protein product-Retained intronNoncoding transcript containing intronic sequence. -
ADAM8-010ENST00000561175481No protein product-Retained intronNoncoding transcript containing intronic sequence. -
ADAM8-011ENST00000559018409No 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.