Description
solute carrier family 18 (vesicular monoamine), member 1 [Source:HGNC Symbol;Acc:10934]
Location
Chromosome 8: 20,002,366-20,040,717 reverse strand.
Transcripts
This gene has 10 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
SLC18A1-001ENST000002763732753ENSP00000276373525Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS6013
SLC18A1-002ENST000002658082770ENSP00000265808493Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS47814
SLC18A1-003ENST000005190261980ENSP00000429664493Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS47814
SLC18A1-005ENST00000522513952ENSP00000428999258Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
SLC18A1-008ENST000003816081419ENSP00000371021472Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS47815
SLC18A1-201ENST000004379802822ENSP00000413361472Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS47815
SLC18A1-202ENST000004409262956ENSP00000387549525Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS6013
SLC18A1-004ENST000005177762770ENSP00000428001385Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
SLC18A1-006ENST00000524272908No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
SLC18A1-007ENST00000519171669No 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.