Description
nudix (nucleoside diphosphate linked moiety X)-type motif 14 [Source:HGNC Symbol;Acc:20141]
Location
Chromosome 14: 105,639,275-105,647,660 reverse strand.
Transcripts
This gene has 8 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
NUDT14-001ENST00000392568845ENSP00000376349222Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS10000
NUDT14-201ENST000005358323328ENSP00000443570149Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
NUDT14-005ENST00000546553527ENSP0000044793396Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
NUDT14-007ENST00000550912541No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
NUDT14-002ENST000005510241042No protein product-Retained intronNoncoding transcript containing intronic sequence. -
NUDT14-003ENST000005505793328No protein product-Retained intronNoncoding transcript containing intronic sequence. -
NUDT14-004ENST00000339418570No protein product-Retained intronNoncoding transcript containing intronic sequence. -
NUDT14-006ENST00000550002456No 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.