Description
synaptic Ras GTPase activating protein 1 [Source:HGNC Symbol;Acc:11497]
Location
Chromosome 6: 33,387,847-33,421,466 forward strand.
Transcripts
This gene has 10 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
SYNGAP1-001ENST000004186005916ENSP000004036361343Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS34434
SYNGAP1-003ENST000004289824339ENSP000004124751284Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
SYNGAP1-009ENST000004493723929ENSP000004165191292Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
SYNGAP1-201ENST000002937484095ENSP000002937481299Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
SYNGAP1-010ENST000004404744764ENSP00000410023902Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
SYNGAP1-004ENST000004963744556No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
SYNGAP1-005ENST00000495633260No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
SYNGAP1-007ENST00000486399479No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
SYNGAP1-002ENST000004795102061No protein product-Retained intronNoncoding transcript containing intronic sequence. -
SYNGAP1-008ENST00000470232394No 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.