Description
leucine-rich repeats and WD repeat domain containing 1 [Source:HGNC Symbol;Acc:21769]
Location
Chromosome 7: 102,105,376-102,113,615 forward strand.
Transcripts
This gene has 9 transcripts
NameTranscript IDLength (bp)Protein IDLength (aa)BiotypeCCDS
LRWD1-001ENST000002926162215ENSP00000292616647Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.CCDS34715
LRWD1-008ENST00000488689635ENSP00000420544212Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
LRWD1-009ENST00000468175847ENSP00000420373242Protein codingA protein coding transcript is a spliced mRNA that leads to a protein product.-
LRWD1-003ENST00000464107646ENSP0000041820445Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
LRWD1-004ENST000004637391062ENSP0000042065027Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
LRWD1-005ENST00000476270703ENSP0000041791341Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
LRWD1-007ENST00000485808908ENSP00000420729179Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins. -
LRWD1-002ENST000004738805491No protein product-Retained intronNoncoding transcript containing intronic sequence. -
LRWD1-006ENST00000485417552No 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.