Description
oxidase (cytochrome c) assembly 1-like [Source:HGNC Symbol;Acc:8526]
Location
Chromosome 14: 23,235,731-23,241,007 forward strand.
Transcripts
This gene has 11 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
OXA1L-001ENST000002858481728ENSP00000285848495Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS9573
OXA1L-003ENST000003580431750ENSP00000350740419Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
OXA1L-006ENST000004127911440ENSP00000387601408Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
OXA1L-009ENST00000431881889ENSP00000396596112Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
OXA1L-008ENST00000442110691ENSP0000038924082Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
OXA1L-002ENST00000473744824No protein product-Retained intronNoncoding transcript containing intronic sequence. -
OXA1L-004ENST000004954241679No protein product-Retained intronNoncoding transcript containing intronic sequence. -
OXA1L-005ENST000004839391224No protein product-Retained intronNoncoding transcript containing intronic sequence. -
OXA1L-007ENST000004812181596No protein product-Retained intronNoncoding transcript containing intronic sequence. -
OXA1L-010ENST00000557299538No protein product-Retained intronNoncoding transcript containing intronic sequence. -
OXA1L-011ENST00000556473593No 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.