Special

GgaINT0011798 @ galGal4

Intron Retention

Gene
Description
laminin, alpha 5 [Source:HGNC Symbol;Acc:HGNC:6485]
Coordinates
chr20:8191592-8192064:-
Coord C1 exon
chr20:8191964-8192064
Coord A exon
chr20:8191773-8191963
Coord C2 exon
chr20:8191592-8191772
Length
191 bp
Sequences
Splice sites
5' ss Seq
GAGGTGAGG
5' ss Score
8.41
3' ss Seq
ACTGACCTGCTTTTCCCTAGGAG
3' ss Score
9.79
Exon sequences
Seq C1 exon
AGTGCAACTGTTCACCTTGTGGGACTGACTCATGCCATCCACAAACCGGCCAGTGCTTCTGCAAGGCTGGAGTGACGGGGCAGCACTGCGACCACTGCGAG
Seq A exon
GTGAGGCTGCCTGTGTACCGCGATGGTACCTTTGCTTGTCACGGGTGCTTCAGCTGCAGCTTTGGCAGTGATGCAGTACCCTATGGGGAGCTGCAGCAAACCTCATTTCCCTGCACGTATCCAGCGTGAGCTGTGCAGGACAAAGGTGGGTTTGCCCTGAACAGGGCCTGCACTGACCTGCTTTTCCCTAG
Seq C2 exon
GAGGGGTACTACGGCTTCGAGGGATGCTCTGGCTGCAGGAGGTGTGACTGTGATGTCGGTGCCATGGGGAGCAGCTGTCACGCACAGACAGGCCAATGCCACTGCCTGCCCGGCGTCAGCGGCTCGCGCTGCCAGCAGTGTGCCCCAGGCTACTGGGGCTTCAGCGAGAGGGGCTGCAGAA
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000005321:ENSGALT00000008535:42
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=PU(71.1=94.1)
A:
NA
C2:
PF0005319=Laminin_EGF=PD(24.4=18.0),PF0005319=Laminin_EGF=PU(92.0=75.4)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CTTGTGGGACTGACTCATGCC
R:
CTCTCGCTGAAGCCCCAGTAG
Band lengths:
256-447
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]