Special

MmuINT0089658 @ mm9

Intron Retention

Gene
Description
laminin, beta 2 [Source:MGI Symbol;Acc:MGI:99916]
Coordinates
chr9:108384839-108385391:+
Coord C1 exon
chr9:108384839-108385027
Coord A exon
chr9:108385028-108385211
Coord C2 exon
chr9:108385212-108385391
Length
184 bp
Sequences
Splice sites
5' ss Seq
GTCGTAAGG
5' ss Score
5
3' ss Seq
TATACTCTCCTTTTTCTCAGCTT
3' ss Score
7.85
Exon sequences
Seq C1 exon
AGTGTGAGTGCAACGGGCATACTCATAGCTGCCACTTTGACATGGCTGTCTACCTGGCATCTGGAAATGTAAGTGGAGGCGTATGCGATGGGTGTCAGCACAACACAGCTGGGCGCCATTGTGAGTTCTGCCGGCCCTTCTTCTACCGTGACCCCACCAAGGACATGCGGGACCCAGCTGTGTGCCGTC
Seq A exon
GTAAGGCTGGGATTGGGCATGAGGGAGGGAAAGCTGAGCCTGCGTCAGGAACTAGGAAGCTGGATTATAGTACCGGTTCCCAGGATTGGTGTGGTCAGGGCTTGGGGTAGAACCAGAACAGGGAAAGGGGAAGGCTCAGGATGGTCACTGCGATGGGGTGACTTTATACTCTCCTTTTTCTCAG
Seq C2 exon
CTTGTGACTGTGACCCTATGGGTTCTCAAGATGGTGGTCGCTGTGATTCTCATGATGACCCTGTGCTAGGACTGGTCTCAGGCCAGTGTCGCTGCAAAGAACACGTGGTTGGCACTCGCTGCCAGCAATGCCGTGATGGCTTCTTTGGACTTAGTGCCAGTGACCCTCGAGGGTGCCAGC
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000052911-Lamb2:NM_008483:10
Average complexity
IR-S
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:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GGGCATACTCATAGCTGCCAC
R:
CCTGAGACCAGTCCTAGCACA
Band lengths:
257-441
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Pre-implantation embryo development
  • Muscular differentiation time course
  • Spermatogenesis cell types
  • Reprogramming of fibroblasts to iPSCs
  • Hematopoietic precursors and cell types