Special

RnoINT0084105 @ rn6

Intron Retention

Gene
Description
laminin subunit beta 2 [Source:RGD Symbol;Acc:2988]
Coordinates
chr8:117270801-117271361:+
Coord C1 exon
chr8:117270801-117270989
Coord A exon
chr8:117270990-117271181
Coord C2 exon
chr8:117271182-117271361
Length
192 bp
Sequences
Splice sites
5' ss Seq
GTCGTAAGG
5' ss Score
5
3' ss Seq
TATACTTTCCTTTTTCTCAGCTT
3' ss Score
8.45
Exon sequences
Seq C1 exon
AGTGTGAGTGCAACGGGCATAGTCATAGCTGCCACTTTGACATGGCTGTGTACCTGGCATCTGGAAACGTAAGTGGAGGTGTCTGCGATGGCTGTCAGCACAACACGGCTGGGCGCCACTGCGAGCTCTGCCGGCCCTTCTTCTACCGTGACCCAACCAAGGACATGCGGGATCCAGCTGCGTGCCGTC
Seq A exon
GTAAGGCTGGGATTGGGCACGAGGGAGGGAAAGCTGAGCCTGAGGCGGGAACTAGGAAGCTAGATTATAGATTACGGTCCTGGTCACCGGGAATTGGTGTGGTAAGGGCTTGGGGGAGAACCAGAGCAGGAGTAGGGGAAGTCTCAGGCTTGTCACTGGGATAGGGTGATTTTATACTTTCCTTTTTCTCAG
Seq C2 exon
CTTGTGACTGTGACCCAATGGGTTCTCAAGACGGTGGCCGCTGTGATTCCCATGATGACCCTGTGCTAGGTCTGGTCTCAGGCCAGTGTCGCTGCAAAGAACACGTGGTTGGCACTCGCTGCCAGCAATGCCGGGACGGCTTCTTTGGACTTAGTGCCAGCAACCCTCGAGGATGTCAGC
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000047768:ENSRNOT00000072098:10
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=WD(100=95.3)
A:
NA
C2:
PF0005319=Laminin_EGF=WD(100=95.1)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GGGCATAGTCATAGCTGCCAC
R:
CCTGAGACCAGACCTAGCACA
Band lengths:
257-449
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]