Special

GgaINT0011761 @ galGal4

Intron Retention

Gene
Description
laminin, alpha 5 [Source:HGNC Symbol;Acc:HGNC:6485]
Coordinates
chr20:8216565-8217225:-
Coord C1 exon
chr20:8217135-8217225
Coord A exon
chr20:8216700-8217134
Coord C2 exon
chr20:8216565-8216699
Length
435 bp
Sequences
Splice sites
5' ss Seq
ATCGTGAGT
5' ss Score
8.88
3' ss Seq
CACTGCTGTCCCCTCTGTAGGTT
3' ss Score
10.29
Exon sequences
Seq C1 exon
CATCACACCACTGGCGTTAACTGTGAGAGATGCATCCCAGGATACTACCGCTCCCCTGACCACCCCATCGACTCTCCATACATTTGCTATC
Seq A exon
GTGAGTGTGATCTCCTCTGCAGTTTATAGACACTCTCCTTTACTTGGTGACTCCGGGATGGGTGTGTGAGATCTCCAGGCAGCAGTGGGTTATGTCTGTCCCAATGGGGAGCCCAGCTTGGTCTGGTGGCTGTGACTGGTGGTGTTCTACCCTGCATCCATCCCTTGAGCCTTCCAGTGCCACCACTGCCTCTCCAGGGGAGACCTGGAGACTCCTGCAGAAGCAAGTTGGGGTTGTGCTGCTTTCCTTGGGACCACGCAGTGTGACAAAGACAGTGGCAGCAATTCCTCTAAGCCAGACTCGTTCTGGAGATGAAAAATCACACTTCTTATTTTTGGAGAGAATTCACAGAATTTGTGGAGCCTCTTCCAAAGACTCTGTGTTGTAGCAGTGCCCCTGTTGTGCTTGTGATGACCACTGCTGTCCCCTCTGTAG
Seq C2 exon
GTTGCAACTGCAAGTCTGACTTCACTGATGGCACCTGTGAGGACCTCACTGGCCGCTGTTACTGCAAACCCAACTACACCGGGGAGCACTGCAATGCCTGTGCTGAGGGATACCTGGACTTCCCCCACTGCTACC
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000005321:ENSGALT00000008535:5
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(41.2=90.3)
A:
NA
C2:
PF0005319=Laminin_EGF=PU(93.6=95.7)


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:
CACACCACTGGCGTTAACTGT
R:
GTAGCAGTGGGGGAAGTCCAG
Band lengths:
222-657
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]