Description
ADAM metallopeptidase domain 9 [Source:HGNC Symbol;Acc:216]
Location
Chromosome 8: 38,854,388-38,962,663 forward strand.
Transcripts
This gene has 9 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
ADAM9-001ENST000004872733839ENSP00000419446819Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS6112
ADAM9-002ENST000004815132387ENSP00000417066128Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
ADAM9-003ENST000004669362053ENSP00000420257147Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
ADAM9-005ENST000004818733793ENSP00000418437712Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
ADAM9-006ENST000004680653755ENSP00000418737628Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
ADAM9-007ENST000003799173836ENSP00000369249655Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
ADAM9-008ENST00000484143658No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
ADAM9-004ENST00000481058516No protein product-Retained intronNoncoding transcript containing intronic sequence. -
ADAM9-010ENST00000463437583No 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.