Description
solute carrier family 14 (urea transporter), member 1 (Kidd blood group) [Source:HGNC Symbol;Acc:10918]
Location
Chromosome 18: 43,304,092-43,332,485 forward strand.
Transcripts
This gene has 7 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
SLC14A1-002ENST000003219253971ENSP00000318546389Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS11925
SLC14A1-201ENST000004029431390ENSP00000385320284Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
SLC14A1-202ENST000004154274129ENSP00000412309445Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS45860
SLC14A1-203ENST000004364074226ENSP00000390637445Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS45860
SLC14A1-204ENST000005020592371ENSP00000442180281Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
SLC14A1-205ENST000005354741048ENSP00000441998257Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
SLC14A1-001ENST000004617631684ENSP00000436061214Nonsense 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.