Description
cytochrome b5 reductase 3 [Source:HGNC Symbol;Acc:2873]
Location
Chromosome 22: 43,013,846-43,045,574 reverse strand.
Transcripts
This gene has 10 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
CYB5R3-001ENST000003523972124ENSP00000338461301Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS33658
CYB5R3-002ENST000004076232153ENSP00000384834278Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS14040
CYB5R3-003ENST000004073321849ENSP00000384457278Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS14040
CYB5R3-006ENST00000438270675ENSP00000403439147Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
CYB5R3-007ENST000004024381050ENSP00000385679278Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS14040
CYB5R3-201ENST000003617402938ENSP00000354468334Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS54535
CYB5R3-202ENST000003963032922ENSP00000379597278Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS14040
CYB5R3-004ENST000004145871710ENSP00000415224124Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
CYB5R3-005ENST000004707413938No protein product-Retained intronNoncoding transcript containing intronic sequence. -
CYB5R3-008ENST00000466276581No 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.