Description
anterior pharynx defective 1 homolog B (C. elegans) [Source:HGNC Symbol;Acc:24080]
Location
Chromosome 15: 63,568,217-63,601,325 forward strand.
Transcripts
This gene has 10 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
APH1B-001ENST000002618794189ENSP00000261879257Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS10184
APH1B-002ENST00000380343685ENSP00000369700216Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS45276
APH1B-005ENST00000560353672ENSP00000453327222Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
APH1B-006ENST00000560890758ENSP00000453002189Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
APH1B-003ENST00000380340872ENSP0000036969781Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
APH1B-004ENST000005599711455ENSP0000045351619Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
APH1B-008ENST00000560716731No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
APH1B-009ENST00000559823376No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
APH1B-010ENST00000559744456No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
APH1B-007ENST00000558631515No 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.