Description
tripartite motif containing 22 [Source:HGNC Symbol;Acc:16379]
Location
Chromosome 11: 5,710,919-5,758,319 forward strand.
Transcripts
This gene has 13 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
TRIM22-001ENST000003799652989ENSP00000369299498Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS41612
TRIM22-003ENST00000425490812ENSP00000400417203Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
TRIM22-005ENST00000414641897ENSP00000396849227Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
TRIM22-006ENST000004548281002ENSP00000393250305Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
TRIM22-008ENST00000450670508ENSP0000040641263Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
TRIM22-010ENST000004290631241ENSP0000040999137Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
TRIM22-011ENST000004448441244ENSP0000040420438Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
TRIM22-201ENST000004552932477ENSP00000412845420Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
TRIM22-202ENST000005453381688ENSP00000444378309Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
TRIM22-007ENST00000414897655ENSP00000388994143Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
TRIM22-002ENST000004803952008No protein product-Retained intronNoncoding transcript containing intronic sequence. -
TRIM22-004ENST00000460454926No protein product-Retained intronNoncoding transcript containing intronic sequence. -
TRIM22-009ENST00000493494460No 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.