Description
EPH receptor B6 [Source:HGNC Symbol;Acc:3396]
Location
Chromosome 7: 142,552,792-142,568,847 forward strand.
Transcripts
This gene has 10 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
EPHB6-001ENST000004421294008ENSP000004107891021Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS5873
EPHB6-201ENST000003929574043ENSP000003766841021Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS5873
EPHB6-202ENST000004114712425ENSP00000409061744Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
EPHB6-003ENST000004259953858ENSP0000041117550Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
EPHB6-004ENST000004226433126ENSP00000404786183Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
EPHB6-008ENST00000476059655No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
EPHB6-009ENST00000497095552No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
EPHB6-002ENST000004667834406No protein product-Retained intronNoncoding transcript containing intronic sequence. -
EPHB6-005ENST000004865112300No protein product-Retained intronNoncoding transcript containing intronic sequence. -
EPHB6-007ENST00000471581475No 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.