Description
thyroid stimulating hormone receptor [Source:HGNC Symbol;Acc:12373]
Location
Chromosome 14: 81,421,333-81,612,646 forward strand.
Transcripts
This gene has 10 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
TSHR-001ENST000005411584566ENSP00000441235764Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS9872
TSHR-003ENST000003424431281ENSP00000340113253Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS32131
TSHR-004ENST000005542631184ENSP00000451202231Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
TSHR-005ENST000005544351089ENSP00000450549274Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS55935
TSHR-201ENST000002981714400ENSP00000298171764Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS9872
TSHR-202ENST000004124291664ENSP00000410839411Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
TSHR-008ENST00000555326557ENSP00000451092112Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
TSHR-006ENST00000557096633No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
TSHR-007ENST00000553763562No protein product-Retained intronNoncoding transcript containing intronic sequence. -
TSHR-009ENST00000556031333No 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.