Special

GgaINT0011769 @ galGal4

Intron Retention

Gene
Description
laminin, alpha 5 [Source:HGNC Symbol;Acc:HGNC:6485]
Coordinates
chr20:8210401-8210769:-
Coord C1 exon
chr20:8210717-8210769
Coord A exon
chr20:8210501-8210716
Coord C2 exon
chr20:8210401-8210500
Length
216 bp
Sequences
Splice sites
5' ss Seq
CCAGTGAGT
5' ss Score
8.28
3' ss Seq
TTTCTCCTCCATTTCTCCAGGGC
3' ss Score
10.49
Exon sequences
Seq C1 exon
TGGGCTCCTGTAACCCAGCTGGGTTAGTGACTGCAGATCCCTCGCTGGCCCCA
Seq A exon
GTGAGTATCATCAGATGAACCTGCCCAACCTCTGCAGGCCGTTTTATTTATTTATTTATTTATTTATTTGCACGATCCCTCTTTTTCTTGCTTGGGCCAAATCATTCCTAAAGCACAGTTCTAGAAGCAGCCGTTGCTCACTCTCGGGTAGCAGACACTATGTTCAGCCACTGTTATGCAAATTCTCACCTGCTCTTTTCTCCTCCATTTCTCCAG
Seq C2 exon
GGCTCCTGTGCATGTCGGGCATACGTTGAAGGCCCAGCTTGTGACAGATGCAAGCCCTTGTACTGGAACCTGACTCCAGATAACCCTTATGGCTGCACGA
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000005321:ENSGALT00000008535:13
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0005319=Laminin_EGF=PD(6.1=16.7)
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
GGGCTCCTGTAACCCAGCT
R:
TCGTGCAGCCATAAGGGTTAT
Band lengths:
152-368
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]