Description
progesterone receptor [Source:HGNC Symbol;Acc:8910]
Location
Chromosome 11: 100,900,355-101,001,255 reverse strand.
Transcripts
This gene has 9 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
PGR-001ENST0000032545513748ENSP00000325120933Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS8310
PGR-002ENST000005340131901ENSP00000436561339Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
PGR-006ENST000002634632496ENSP00000263463831Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
PGR-201ENST000005376232816ENSP00000440871690Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
PGR-004ENST000005289602633ENSP00000432914764Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
PGR-005ENST000005347802750ENSP00000432352803Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
PGR-007ENST000005263002365ENSP00000436803695Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
PGR-008ENST000005332072224No protein product-Retained intronNoncoding transcript containing intronic sequence. -
PGR-009ENST00000530764620No 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.