Description
pecanex-like 2 (Drosophila) [Source:HGNC Symbol;Acc:8736]
Location
Chromosome 1: 233,119,881-233,431,459 reverse strand.
Transcripts
This gene has 23 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
PCNXL2-001ENST000003446985348ENSP00000340759777Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
PCNXL2-002ENST000002582296817ENSP000002582292137Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS44335
PCNXL2-010ENST000004887801465ENSP00000430820424Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
PCNXL2-011ENST00000484347803ENSP00000428134178Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
PCNXL2-019ENST00000518351545ENSP00000429231182Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
PCNXL2-201ENST000004301533199ENSP00000394703286Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
PCNXL2-005ENST000004754632183ENSP00000429360218Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
PCNXL2-007ENST000004622333392ENSP00000428488490Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
PCNXL2-012ENST00000486012654ENSP0000042858247Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
PCNXL2-018ENST00000517808307ENSP0000042926245Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
PCNXL2-022ENST00000490102561ENSP00000427962109Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
PCNXL2-008ENST00000467336747No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
PCNXL2-015ENST00000496675598No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
PCNXL2-016ENST00000462762383No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
PCNXL2-020ENST00000496510551No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
PCNXL2-021ENST00000520463766No protein product-Processed transcriptNoncoding transcript that does not contain an open reading frame (ORF). -
PCNXL2-003ENST000003241421828No protein product-Retained intronNoncoding transcript containing intronic sequence. -
PCNXL2-009ENST00000498302486No protein product-Retained intronNoncoding transcript containing intronic sequence. -
PCNXL2-013ENST00000484041625No protein product-Retained intronNoncoding transcript containing intronic sequence. -
PCNXL2-014ENST00000497623639No protein product-Retained intronNoncoding transcript containing intronic sequence. -
PCNXL2-017ENST00000519530439No protein product-Retained intronNoncoding transcript containing intronic sequence. -
PCNXL2-023ENST00000429988559No protein product-Retained intronNoncoding transcript containing intronic sequence. -
PCNXL2-024ENST00000522067569No 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.