Special

GgaINT0011786 @ galGal4

Intron Retention

Gene
Description
laminin, alpha 5 [Source:HGNC Symbol;Acc:HGNC:6485]
Coordinates
chr20:8197113-8197742:-
Coord C1 exon
chr20:8197531-8197742
Coord A exon
chr20:8197318-8197530
Coord C2 exon
chr20:8197113-8197317
Length
213 bp
Sequences
Splice sites
5' ss Seq
GGCGTAAGT
5' ss Score
9.39
3' ss Seq
CTCCTTTTTGTCTCTTGCAGCCT
3' ss Score
12.15
Exon sequences
Seq C1 exon
TCCCAGCACATCGTCGAGGTTTTGCCGTGACTCCGCCATCTCGCTGTCCCTCTTCTACAACAATGGGGCACAGCCCTGCCAGTGCCATGAGGCGGGGGCACGGGGCAGCCAGTGCGAGCCCTTTGGTGGGCAGTGTCCCTGCAAGTCCAATGTCATCGGGCGAGAGTGCTCCCGCTGCGCCACCGGCTACTGGGGCTTCCCCAACTGCAGGC
Seq A exon
GTAAGTTGTCCTGTCTCCTGCCCTGCTTTCTGCAGCACTGACTGCTTGGCCTCTTTTGGGGCAAAGACAGAATTGGAAACGCTTGCATTTTCCAGCCCTGAAACGGCTTCAGGAAGGCAGCCCAGCCCCCTGCAGAGCCTCCGTTGCCCTGTGCCTTCCTTGGGTTGCGTGGCTCTTGCTTTTCCAAACACACCTCCTTTTTGTCTCTTGCAG
Seq C2 exon
CCTGTGACTGTGGGACACGACTCTGCGACGAGGTGACAGGGCAGTGCATCTGCCCTCCTCACACCCTGAAGCCAGAATGTGTTGTCTGTGAGCCCCAGACCTTCGGTTGCCATCCCCTCATCGGCTGTGAGGACTGCAATTGCTCGCAGCCTGGAGTGCAGGAGCTGACAGAGCTTGGCTGTGATGTGGACAGCGGGCAGTGCAA
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000005321:ENSGALT00000008535:30
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(91.8=62.5)
A:
NA
C2:
PF0005319=Laminin_EGF=PD(6.1=4.3),PF0005319=Laminin_EGF=PU(46.9=33.3)


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:
TCTACAACAATGGGGCACAGC
R:
CGAGCAATTGCAGTCCTCACA
Band lengths:
305-518
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]