Special

GgaEX1032846 @ galGal4

Exon Skipping

Gene
Description
laminin, alpha 5 [Source:HGNC Symbol;Acc:HGNC:6485]
Coordinates
chr20:8196108-8197317:-
Coord C1 exon
chr20:8197113-8197317
Coord A exon
chr20:8196756-8196900
Coord C2 exon
chr20:8196108-8196248
Length
145 bp
Sequences
Splice sites
3' ss Seq
GTCTTTTGCATCCTGCTCAGGTG
3' ss Score
7.91
5' ss Seq
AAGGTCAGT
5' ss Score
8.68
Exon sequences
Seq C1 exon
CCTGTGACTGTGGGACACGACTCTGCGACGAGGTGACAGGGCAGTGCATCTGCCCTCCTCACACCCTGAAGCCAGAATGTGTTGTCTGTGAGCCCCAGACCTTCGGTTGCCATCCCCTCATCGGCTGTGAGGACTGCAATTGCTCGCAGCCTGGAGTGCAGGAGCTGACAGAGCTTGGCTGTGATGTGGACAGCGGGCAGTGCAA
Seq A exon
GTGTAAGCCCAATGTAATTGGGCGACGGTGTGACCTCTGTGCCCCTGGCTACTACCACTATCCCAGCTGTCGGCGGTGTGACTGCCATCCTGATGGCACCGAAGTGAGCGTGTGTGACCCGGTGACGGGGCAGTGTCACTGCAAG
Seq C2 exon
GAAAATGTGGAGGGTCCGAGGTGTGACCAGTGCCGCCTGGGGACGTTTTCTTTGGATGCCAGCAACCCCAAGGGGTGCACCAAGTGTTTCTGCTTTGGTGCCACCAATCGCTGCCGCAGTGCTGTGAAGTACCGAGCTGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000005321-'40-50,'40-48,41-50
Average complexity
S
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

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

C1:
PF0005319=Laminin_EGF=PD(6.1=4.3),PF0005319=Laminin_EGF=PU(46.9=33.3)
A:
PF0005319=Laminin_EGF=PD(51.0=51.0),PF0005319=Laminin_EGF=PU(44.9=44.9)
C2:
PF0005319=Laminin_EGF=PD(51.0=53.2)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CACCCTGAAGCCAGAATGTGT
R:
TGGCACCAAAGCAGAAACACT
Band lengths:
247-392
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]