Description
transient receptor potential cation channel, subfamily C, member 7 [Source:HGNC Symbol;Acc:20754]
Location
Chromosome 5: 135,548,999-135,701,225 reverse strand.
Transcripts
This gene has 9 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
TRPC7-001ENST000005131042987ENSP00000426070862Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS47267
TRPC7-003ENST000003521892239ENSP00000330322746Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
TRPC7-005ENST000003784592404ENSP00000367720801Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
TRPC7-006ENST000005027532422ENSP00000424854807Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
TRPC7-201ENST000003551802752ENSP00000347312801Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS54906
TRPC7-202ENST000004260572587ENSP00000441628746Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS54905
TRPC7-002ENST000005032752603ENSP00000421571380Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
TRPC7-004ENST000005149632022ENSP00000426870261Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
TRPC7-007ENST00000509288817No 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.