Description
family with sequence similarity 189, member B [Source:HGNC Symbol;Acc:1233]
Location
Chromosome 1: 155,216,996-155,225,274 reverse strand.
Transcripts
This gene has 11 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
FAM189B-001ENST000003613613082ENSP00000354958668Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS1103
FAM189B-002ENST000003502102379ENSP00000307128572Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS1104
FAM189B-004ENST000003683682609ENSP00000357352650Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
FAM189B-008ENST000004910821006ENSP00000427011325Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
FAM189B-201ENST000003233612550ENSP00000323164357Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
FAM189B-202ENST000003339661386ENSP00000333944242Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
FAM189B-007ENST000004876491499ENSP00000427520144Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
FAM189B-010ENST00000472550948No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
FAM189B-003ENST000003683661962No protein product-Retained intronNoncoding transcript containing intronic sequence. -
FAM189B-006ENST000004818222103No protein product-Retained intronNoncoding transcript containing intronic sequence. -
FAM189B-009ENST00000497941871No 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.