Special

MmuINT0049595 @ mm10

Intron Retention

Gene
Description
disco interacting protein 2 homolog B [Source:MGI Symbol;Acc:MGI:2145977]
Coordinates
chr15:100206397-100207832:+
Coord C1 exon
chr15:100206397-100206454
Coord A exon
chr15:100206455-100207757
Coord C2 exon
chr15:100207758-100207832
Length
1303 bp
Sequences
Splice sites
5' ss Seq
AAGGTATTC
5' ss Score
6.8
3' ss Seq
ATTTCCTCTTTGATTCTTAGATC
3' ss Score
8.97
Exon sequences
Seq C1 exon
GGTCCGTCTTGTGGAACGGGGTGCCCCCCAGAGCCTCCTGCTTTCTGAATCTGGAAAG
Seq A exon
GTATTCTATTCTGCTAGCTGCTGGGGAAGGCTGGGATGGAGGAAGAGGGCTGAAGCCTGAGAGAAGAGTCCAGTCAAGCTTAGAGAAAAGCCCATAGGCTTTCCTTAATGGATGGTTTCAGATGCATGAAGACCAGATGTGCACTTATCTCCAGATTGTTTAAATCCCATGGACACGCCATTCTTACTGATAAGCCAGCAAAGTGGCTAGAGGGGCAGCACCTGAGGAAGCCAGCTCTGTCTGTAAACACTGAAAGTCAGGACAGAGAGGAGCTTCGAGAAAGAGAGCTAGAGAGCTAGCAGCTACTCTGAGCATCCCTTCACCCTATCCCCTCCATCCTCACCACCTCCCCCTCTGTCATCCCTCACCCTGAACTGTCCAGACAGAGGACAGAATTGAGAAGATGTGTCAGGGTCCTGCCTAGGAATCCTGAGGCAGAGAAGAAAGAAACCCAAAGGAGACTCTGCCTACTCTCCAGCATATGTCACAACACAGGGGGCTTGTGTGAACTGCGTGTGTGGGCTGTGCCATTCATTGCTCATGTCTGCAGTTGGGAGCACGTGGAAGCAGGAATATCATGTCATGAGGGTAGGCCGAGGCTACCCTTTATTCCCTTCCTCTAGGTTTTAGATACTTAAACCTGGGTAGTAAGTCTCAGGCTTTAGAAACCCAAGCTAAAAAATTAACAGGGCAAGAGACAGTAACCCAAATGGCTGGATGACTCTCTTGCCTGTTTGCCCAGAATGGTCCTCGTCCATAGTAGGCAAGTGGCTTACTGCTGAACTACACTACTACCGTGGAATCATCTTAGGTGAGCCCTCATCCATGAGCCCAGACAGCATATGTTTCTCTTCCTCCCTATTGTGGCTCCCCACTGTAGTCTGAGCTCCCCGTGGAGTGGTCTCCAAGTTCTCCTCCTAGTTTATCTTTGGAAAGGCTTACCCAAAAGGGAATGGCTGAGATACTTACCAGCGTCTTGCTGTTGTGGCCTTGAGCAGAAGTTTCTCAACCCTCTGAGGAGATAGCAGTCTGGATTGTTCTAGCTTCAGAGTGGAACTCACTGATCCTCCATCTCTACTAAGACGAGAAAGATTGACCAGGAACAAACAGAAAAGCACTTCAGGACCCTTTGAGTGATGGCTGCTTCATTAGCTCTTGCCATTTCTAGTCCAGTTCCTAGAGGTCATTGGTTGATTGCAGGGCTTGGGGTTAGAAGCCATGCCTCAGACCAGTAAGCTAAGCCACAGCCACAGGTACGAGGCTTGGTTGAACTGAGTATTTGTATTTCCTCTTTGATTCTTAG
Seq C2 exon
ATCTTACCTGGAGTAAAAGTAGTTATTGTCAATCCTGAGACCAAAGGACCTGTTGGAGACTCTCACCTGGGAGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000023026:ENSMUST00000100203:34
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.050 A=NA C2=0.080
Domain overlap (PFAM):

C1:
PF0050123=AMP-binding=PD(4.3=80.0)
A:
NA
C2:
PF0050123=AMP-binding=FE(5.0=100)


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:
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]


SPECIAL DATASETS

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