Special

MmuINT0109817 @ mm10

Intron Retention

Gene
Description
notch 3 [Source:MGI Symbol;Acc:MGI:99460]
Coordinates
chr17:32132202-32133692:-
Coord C1 exon
chr17:32133388-32133692
Coord A exon
chr17:32132350-32133387
Coord C2 exon
chr17:32132202-32132349
Length
1038 bp
Sequences
Splice sites
5' ss Seq
CAGGTGAGA
5' ss Score
9.22
3' ss Seq
ATGGCTTTTGTCGTCGTTAGATT
3' ss Score
6.93
Exon sequences
Seq C1 exon
ATGGCTTCACCCCACTTATGCTGGCCTCCTTCTGTGGGGGAGCCCTGGAGCCGATGCCAGCTGAGGAGGATGAGGCGGATGACACATCAGCCAGCATTATCTCAGATCTGATCTGTCAAGGGGCCCAGCTCGGGGCACGGACTGACCGCACTGGCGAGACCGCCCTGCATTTGGCTGCCCGCTATGCTAGAGCGGATGCAGCCAAGCGTCTCCTGGATGCTGGGGCGGACACCAACGCCCAGGATCATTCGGGCCGCACCCCCCTGCACACCGCAGTGACAGCTGATGCCCAGGGTGTCTTCCAG
Seq A exon
GTGAGACAGGCCTGTCTCTTCAGACTGCAGAGCTGCTGGGAGGGGATCAGACACACCTAGATTGGAGCCCCGGTCTGTCTTGCAAGGCTTTTGTCATTTGGAAATAGGAATAGGTAGTATCTCACCTAGATTTCCCGCCGGCCCCCCCCCCCCCCCCCCAGGACAGGGTTTCTGTATAGTCCTGGCTGTGCTAGAACTCACTCCAATAAACCAGGCTGGCCTCGAACTCAGAAAGATCCACTTGCCTCTGCCTCTGGAGTGCTAGGATTAAAGGCATGCACCACTAACACTGGATAGAATTTTTTTCTTTTTTAATTTTATTAATATATGTAAGTACACTGTAGCTGTCTTCAGACACTCCAGAAGAGGGAGTCAGAACTTGTTGCAGATGGTTGTAAGCCACCATGTGGTTGCTGGGATTTGAACTCTGGACCTTCGGAAGAGCAGTCGGGTGCTCTTACCCACTGAGCCATCTCACCAGCCCTGGATAGAATTTTTTAAAAAGTATCATTAAAATTACATTTATTTGGTGTGTGTGTGTATGTTATGCTGATTGGTTTGTGTTTGTTTGTGTGGCATATGTGTACCTGGGTATGTACATTGCCCAGCTTGCTGAAGCTAGAGGAGGCTGTTGATTGTTCTGCTCTATCGTGCTCCACCCAATCTTTTGAGACAGAGCCCATCAGCGAGCCTGGAGTTGAGCTGGTGTCCAGAAAGCTCTCTTGATCCTCTTGTCTTCTTCCCCACAGCCCTGGGGCACACATGACCAAGACTGGCTTTTTAGGTGGACTTTGGGCTCTGACGTCAGGTGCTTGTCCCCTGAGCCATCTCCCTGTCCTTCCATATCATACTGTTACTTAAATCCATTTTGAATGAGCATATTTTTTGATTTATAATGTGCTTAGCAGGAATAGCACCTCATTTTAAGTCAGGAGATATCTGTAGCTCCTGGGTTCCAAAGCTGTGGCATTTGGGGTTCAGGGTGTGGTATACTCCTCCCTTGGCATAATGTCCTGCCATGGCTTTTGTCGTCGTTAG
Seq C2 exon
ATTCTCATCAGGAACCGCTCCACTGACCTGGATGCCCGAATGGCAGATGGCTCTACTGCACTGATCCTGGCAGCCCGCCTGGCAGTGGAGGGCATGGTGGAAGAGCTCATCGCCAGCCATGCCGATGTCAATGCAGTGGATGAGCTTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000038146:ENSMUST00000087723:30
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.373 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF127962=Ank_2=PU(83.7=75.5)
A:
NA
C2:
PF127962=Ank_2=PD(14.1=26.0),PF127962=Ank_2=PU(30.9=58.0)


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:
GGATGAGGCGGATGACACATC
R:
GATGAGCTCTTCCACCATGCC
Band lengths:
349-1387
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