Special

HsaINT0090429 @ hg19

Intron Retention

Gene
Description
laminin, beta 2 (laminin S) [Source:HGNC Symbol;Acc:6487]
Coordinates
chr3:49167272-49167852:-
Coord C1 exon
chr3:49167664-49167852
Coord A exon
chr3:49167452-49167663
Coord C2 exon
chr3:49167272-49167451
Length
212 bp
Sequences
Splice sites
5' ss Seq
GCTGTGAGG
5' ss Score
2.85
3' ss Seq
GTATCTCTTTTTGCCGTCAGCCT
3' ss Score
3.96
Exon sequences
Seq C1 exon
AGTGTGAGTGCCATGGGCACACCCACAGCTGCCACTTCGACATGGCCGTATACCTGGCATCTGGCAATGTGAGTGGAGGTGTGTGTGATGGATGTCAGCATAACACAGCTGGGCGCCACTGTGAGCTCTGTCGGCCCTTCTTCTACCGTGACCCAACCAAGGACCTGCGGGATCCGGCTGTGTGCCGCT
Seq A exon
GTGAGGCTGGGATTGGGCACGGGGAGAGAAAGCTGAGCCTGGGGCAGGAACTAGAGAGCTGGACTGCTGTCTAAATTGCAGGAAATTGGGGTTAGGGGCTTGGGATAGAACTTGACCAGGGATCCAGGGTGGGATCCCTTAGGCTTAGGAGAGGACTGGCAGTGAGCTAGTTGAGATAGGGTGAGTGACCCTGTATCTCTTTTTGCCGTCAG
Seq C2 exon
CCTGTGATTGTGACCCCATGGGTTCTCAAGACGGTGGTCGCTGTGATTCCCATGATGACCCTGCACTGGGACTGGTCTCCGGCCAGTGTCGCTGCAAAGAACATGTGGTGGGCACTCGCTGCCAGCAATGCCGTGATGGCTTCTTTGGGCTCAGCATCAGTGACCGTCTGGGCTGCCGGC
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000172037-LAMB2:NM_002292:9
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:
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GCATCTGGCAATGTGAGTGGA
R:
GTCACTGATGCTGAGCCCAAA
Band lengths:
297-509
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains
  • Pre-implantation embryo development