Description
mitochondrial ribosomal protein S28 [Source:HGNC Symbol;Acc:14513]
Location
Chromosome 8: 80,830,952-80,942,524 reverse strand.
Transcripts
This gene has 10 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
MRPS28-001ENST00000276585850ENSP00000276585187Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS6226
MRPS28-007ENST00000521605437ENSP0000042796586Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
MRPS28-008ENST00000519120403ENSP00000428744103Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
MRPS28-009ENST00000520946411ENSP00000430401109Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
MRPS28-010ENST00000521434585ENSP00000428880125Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
MRPS28-011ENST00000519386555ENSP00000428050143Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
MRPS28-012ENST00000518271487ENSP00000427846163Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
MRPS28-005ENST00000522938657ENSP0000043085894Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
MRPS28-013ENST00000522987487No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
MRPS28-002ENST00000518371604No 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.