Special

MmuINT0142209 @ mm10

Intron Retention

Gene
Description
SET domain, bifurcated 1 [Source:MGI Symbol;Acc:MGI:1934229]
Coordinates
chr3:95327208-95328717:-
Coord C1 exon
chr3:95328548-95328717
Coord A exon
chr3:95327837-95328547
Coord C2 exon
chr3:95327208-95327836
Length
711 bp
Sequences
Splice sites
5' ss Seq
CAGGTTAGT
5' ss Score
8.02
3' ss Seq
TCAATTCTCTTGATTCTCAGGCA
3' ss Score
6.75
Exon sequences
Seq C1 exon
GGTTTATGAGTGTAACAAACGCTGCAATTGTGACCCAAACATGTGCACAAATCGGTTGGTGCAGCATGGTCTGCAGGTTCGACTACAGCTGTTTAAGACACAGAACAAGGGCTGGGGTATCCGCTGCTTGGATGATATTGCCAAAGGCTCTTTTGTCTGCATTTATGCAG
Seq A exon
GTTAGTGATTAAAAAAGGGGTTTTACCCTATGAGGTTTGGGACATGGAAGGTCAAGGAAAAGTTGAACATAGCAAAGTGTTAGTGGGTATGGTAGCACATGTCTATAATCCAAGCACTCAGAAGATGAAAACAGAAAACTTTAAGAGTAGGAGATAACCTGGGCTACAGAGTTAGATTTTACCTCACAAAAAAAAAACAAAACAAAACAGTGTTTGAGGAGTGGAAATGTAGCTCAGGAGAACAATGCATGCTTAGTTTTCAGGAGGTGCTGGATCACTCCCTAACATTAAAAAAAAGAAAGGATGGATGGATGCATAAAGTGTTTGACAGTTGAACTGGGAATAAGAGGAGGTGGGAATCTCTTCTATAAAGGACATGATAAGTGATATATACCTGAATAGGTAGGACCAGAGAGGGGCAAAGGTACTTCTTAAACAGTAGAAGGGAATCAGATTTTGGCTATTGATGTTTCTTTCAGTGAGAGACATCATTTAATTGTATTATTTTCTCCGAGAGATATTTTAACCCAGGAAGTACCAAGGAGGTAAACAAAAGAAAAAAGAAAAAAAAAAATTGGGAAGGGCAAAGCAACAAGCTGCAGTGACATTGACTTAATGTCAGAGGCAAAGGTGGCAAAGTAAGCATATAATAGATTTACCCTGCTGGTGGGTGTAGTACTGATGAAGACCATCAATTCTCTTGATTCTCAG
Seq C2 exon
GCAAAATCCTGACAGATGACTTTGCAGACAAAGAAGGCCTGGAGATGGGTGATGAGTACTTTGCAAATCTGGACCACATTGAAAGTGTGGAGAACTTCAAGGAAGGATATGAGAGTGATGTCCCCACTTCCTCTGACAGCAGTGGGGTAGATATGAAGGACCAGGAAGATGGCAACAGCGGTTCAGAGGACCCTGAAGAATCCAATGATGACAGCTCTGATGATAACTTCTGTAAGGATGAGGACTTCAGCACCAGTTCAGTGTGGCGTAGCTATGCTACCCGGAGGCAGACTCGGGGTCAAAAGGAGAATGAATTGTCTGAGATGACTTCCAAGGACTCCCGCCCCCCAGACCTCGGGCCTCCACATGTTCCTATCCCTTCCTCAGTATCTGTAGGGGGCTGCAATCCACCTTCCTCTGAAGAGACACCCAAGAACAAGGTGGCCTCGTGGTTGAGTTGCAATAGTGTCAGTGAAGGTGGATTTGCTGACTCTGACAGCCGTTCTTCCTTCAAGACTAGTGAAGGTGGAGATGGCCGTGCTGGGGGAGGCCGGGGAGAGGCTGAAAGGGCCTCTACCTCAGGATTGAGCTTCAAGGATGAAGGAGACAATAAGCAGCCTAAAAAAGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000015697:ENSMUST00000107170:15
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=0.810
Domain overlap (PFAM):

C1:
PF0503311=Pre-SET=PD(15.7=31.0),PF0085623=SET=PU(4.4=34.5)
A:
NA
C2:
PF0085623=SET=FE(46.2=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:
CTGCAGGTTCGACTACAGCTG
R:
TGGTGCTGAAGTCCTCATCCT
Band lengths:
355-1066
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