Special

GgaINT0011770 @ galGal4

Intron Retention

Gene
Description
laminin, alpha 5 [Source:HGNC Symbol;Acc:HGNC:6485]
Coordinates
chr20:8209807-8210500:-
Coord C1 exon
chr20:8210401-8210500
Coord A exon
chr20:8209860-8210400
Coord C2 exon
chr20:8209807-8209859
Length
541 bp
Sequences
Splice sites
5' ss Seq
CGAGTAAGG
5' ss Score
6.93
3' ss Seq
GTTCATCTTCCCCTCTCCAGGCT
3' ss Score
9.08
Exon sequences
Seq C1 exon
GGCTCCTGTGCATGTCGGGCATACGTTGAAGGCCCAGCTTGTGACAGATGCAAGCCCTTGTACTGGAACCTGACTCCAGATAACCCTTATGGCTGCACGA
Seq A exon
GTAAGGAAATGGCAAATGCACAACCCCAGAAAGTCCTTTCCGCACTGTAGTGGTACAAGGTTCAAACCCAAGCCAGTGGGGACCACCACTGTTTGATGGAAGTGATATCTTTCCTTCCCTCTTACCGTGAGATATGTCAGTGCTGGAGGTATCTGGGACACCTCTTGGAGAGAGGGAAGGCTAGAGGCTGGAGCTTTTTGCTTGGGGTGGAACACAGAACTTGTGCAATGAGTTGTGCCATTTTCAGCCCTCCCTGAAGACCTTGCACACTTAGACTTTCATGGCCCAATGCGAAGAAAAGTCTAGTGTCTTTGACAATTGTATCTGCAATGGAAACTCATGGTGCAACGGTAACTCAAATGGTAACAATGTCCAAAATGAAAAGTGTGCCCTTGTACAATGCTACCCTTTACTTGACCAGCTCCCAGGTCCTATTATCCCAGGCAGCGTCCTTTGGTATGGTGGGTAATGATCACCCATCACGCTTCTTCTCAGGTGCTGAATGCTCTTCTGACTTTCTTGTTCATCTTCCCCTCTCCAG
Seq C2 exon
GCTGCAAGTGTGAGACCAAGGGCACCATCAGTGGAATTGCAGAGTGTCAGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000005321:ENSGALT00000008535:14
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:
NO
A:
NA
C2:
PF0005319=Laminin_EGF=PU(31.4=88.9)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]