Description
N-ethylmaleimide-sensitive factor [Source:HGNC Symbol;Acc:8016]
Location
Chromosome 17: 44,668,035-44,834,830 forward strand.
Transcripts
This gene has 10 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
NSF-001ENST000003982383983ENSP00000381293744Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS42354
NSF-005ENST000005750682667ENSP00000458221739Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
NSF-008ENST00000571172569ENSP00000458184161Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
NSF-009ENST00000576040364ENSP0000046015244Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
NSF-011ENST00000576346710ENSP00000459646136Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
NSF-201ENST000002252822738ENSP00000225282644Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
NSF-006ENST000005715102223ENSP0000045939357Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
NSF-010ENST00000571864548ENSP0000046144881Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
NSF-003ENST00000465370580No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
NSF-002ENST00000486366447No 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.