Special

GgaINT0011787 @ galGal4

Intron Retention

Gene
Description
laminin, alpha 5 [Source:HGNC Symbol;Acc:HGNC:6485]
Coordinates
chr20:8196756-8197317:-
Coord C1 exon
chr20:8197113-8197317
Coord A exon
chr20:8196901-8197112
Coord C2 exon
chr20:8196756-8196900
Length
212 bp
Sequences
Splice sites
5' ss Seq
CAAGTGAGG
5' ss Score
5.85
3' ss Seq
GTCTTTTGCATCCTGCTCAGGTG
3' ss Score
7.91
Exon sequences
Seq C1 exon
CCTGTGACTGTGGGACACGACTCTGCGACGAGGTGACAGGGCAGTGCATCTGCCCTCCTCACACCCTGAAGCCAGAATGTGTTGTCTGTGAGCCCCAGACCTTCGGTTGCCATCCCCTCATCGGCTGTGAGGACTGCAATTGCTCGCAGCCTGGAGTGCAGGAGCTGACAGAGCTTGGCTGTGATGTGGACAGCGGGCAGTGCAA
Seq A exon
GTGAGGAAGCCCTGTCTCTGTGCAGGGCACAGCTGGCAGTATCTCTAGTTGCTGCTGGGGTGATCGGAAACACTGGAAGGGTGCAGGGAGGAAACGGGCAGGATAGGGAAATCCTTGTCAGCACTGTGCGCCTCCCAGCACGGATGAAGCTTTGCAAATGCAGCAGCATAAAGCATAGGTTTCTAATGCTACGTCTTTTGCATCCTGCTCAG
Seq C2 exon
GTGTAAGCCCAATGTAATTGGGCGACGGTGTGACCTCTGTGCCCCTGGCTACTACCACTATCCCAGCTGTCGGCGGTGTGACTGCCATCCTGATGGCACCGAAGTGAGCGTGTGTGACCCGGTGACGGGGCAGTGTCACTGCAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000005321:ENSGALT00000008535:31
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=4.3),PF0005319=Laminin_EGF=PU(46.9=33.3)
A:
NA
C2:
PF0005319=Laminin_EGF=PD(51.0=51.0),PF0005319=Laminin_EGF=PU(44.9=44.9)


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:
GACTCTGCGACGAGGTGACAG
R:
CACTTCGGTGCCATCAGGATG
Band lengths:
293-505
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]