Special

RnoINT0084022 @ rn6

Intron Retention

Gene
Description
laminin subunit alpha 5 [Source:RGD Symbol;Acc:621023]
Coordinates
chr3:175567616-175568061:-
Coord C1 exon
chr3:175567917-175568061
Coord A exon
chr3:175567757-175567916
Coord C2 exon
chr3:175567616-175567756
Length
160 bp
Sequences
Splice sites
5' ss Seq
AAGGTGAGC
5' ss Score
9.6
3' ss Seq
TGATTGTCCCCTGCCCTTAGGAG
3' ss Score
9.82
Exon sequences
Seq C1 exon
ATGCAGACCCAATGTAGCTGGGCGTCGCTGTGACACCTGTGCACCAGGCTTCTATAGTTATCCTAGCTGTCGCCCCTGTGACTGTCATGAGGCAGGCACCATGGCCAGTGTGTGTGACCCCTTCACAGGCCAGTGCCATTGCAAG
Seq A exon
GTGAGCAGGGGCTTATGTCCAGGTCACCTTCACGGGCCCCTTCCTACAAATCTGCTTCAGCCGACCCATGGACTTCCTGGAAGCTTTTAGGGGGACAAGGCAAAAAAAACGGTCTAAGGTCTGGCTCTCAACACCAGCCTTGATTGTCCCCTGCCCTTAG
Seq C2 exon
GAGAATGTACAGGGCTCCAGATGTGACCAGTGTCGCGTGGGGACCTTCTCCTTGGATGCTGCTAACCCCAAGGGCTGTACCCGCTGCTTCTGTTTCGGAGCCACAGAGCGCTGTGGAAACTCTAACTATGCCCGCCATGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000053691:ENSRNOT00000081226:36
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(51.0=51.0),PF0005319=Laminin_EGF=PU(44.9=44.9)
A:
NA
C2:
PF0005319=Laminin_EGF=PD(51.0=53.2)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
ATGCAGACCCAATGTAGCTGG
R:
TCTGTGGCTCCGAAACAGAAG
Band lengths:
252-412
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]