Special

MmuINT0153120 @ mm9

Intron Retention

Gene
Description
suppression of tumorigenicity 14 (colon carcinoma) [Source:MGI Symbol;Acc:MGI:1338881]
Coordinates
chr9:30907971-30910558:-
Coord C1 exon
chr9:30910461-30910558
Coord A exon
chr9:30908081-30910460
Coord C2 exon
chr9:30907971-30908080
Length
2380 bp
Sequences
Splice sites
5' ss Seq
AAGGTAGGA
5' ss Score
9.45
3' ss Seq
CAAAGCATCTCTCTGTCCAGGTG
3' ss Score
6.79
Exon sequences
Seq C1 exon
GCTGTGGCGGCTTTTTGAGTGACACCCAAGGGACATTTAGCAGCCCCTACTATCCAGGCCACTACCCGCCCAACATCAACTGCACATGGAATATCAAG
Seq A exon
GTAGGAGCAGGTGGCGGCGAGTGCCACGGGACTTGAGGAAAAGCAGGAGGGGAAGATGACATTAACAACCCAGAGAGCCATGTTAACAGGACCCACAAGTCTTTGCTGCAGGACTAGCCACATCCAGACTTGTGTGCCCTAGCTCTTTGATTGACAGCTGAGAGAGCATGGGTGTTTGTCTTCTCTGGATCAGCTTGCTTCTGGGTAAAGTGAGGCTGAAGATCTGTTTCTAAGAGGTGTTGTCCGGATGACCTCACCGAAAGTGTGAAAGAGAGCAAGCCCTAGCACGGCGGTAGTGCTTCTGGGTGCCTCTCGCATCCTCCAATCGGAGGTCTTTCCCTAAAGATGCTGAGGCACCCCATCCTAGCCTTTCAAAGTAACAGAGTACAAATTCCCACACGTGTGCTTATGGTTTTCATTTCCAAGTGGCAGTTATCTGTGGTCAGTCATGATCTGAAAATGTTAGGTGGAAAACTCCAGAAATAAACATGGGCGGGAAGAGTGGGTTTGTTCAGTCGCCCATGCTGGGTGCACTACTTGACTGTTACTTAATACCCGTCATGCTACCACACCGACCGTTGTGTATCACAGGGCTGGCATTCAAGGAATTCTTACTAAATAATGGCCCCCAAATATTAGCTCTTTGGATAAATCACAGAAAATAAAGAAAGTCCTTCCTGCAGGTGAAAAATGTAAATTTTTTTATTTCATTTTTTTTTTTGCTAGATATTTTCTTTATTTACATTTCAAATGTTATCCCCTTTCCTGGTTTCCCCTCCTATTCCCCCCGCCGCCCCATGCTTACCAACCCACCCACTTCCACTTCCTGGCTGTGGCATTCTCCTAAACTGGGGCATAGAACCTTTGCAGGACCAAGGGCCTCTCCTCCCATTGATGTCCGACTAGGCCATCCTCTGCTACATATGCAGCTGGAGCCATGAGTCCCTCCATGTGTTTTCTTTGGTTGTTGGTTTAGTCCCTGGGAGCTCTGGGGATAGTGGTTGGGTCATATTGTTCCTTCTATGGTGCTGCAGACCCCTTCAGCTCCTTAGGTCCTTTCTCTAGCTCCTCCATTGGGGAGGAGGGTGCTCAGCCCTCTGCTCAGTCCAATGGCTGCTTTCGAGCACCCACCTCTGTATTTGTCAGGCACTGGTAGAGCCTCTCAGGAGACAGCTATAACAGACTTCTGTCAGCAAGCACTTGTTGGCATCCACAGTAGTGTCTGGGTTTGGTGACTGTATATGAGATGGATCCCCAGGTGGGGCAGTCTCTGGATGCTCGGTCATACCTTCAGTCTCTGCTCCACACTTTGTAACTCCTTCCATGGGTAATTTATTCCCCTTTCTAAGAAGGACCAAAGTAGCCACACTTTGGTCTTCCTTCTTCTTGAGTTTCATGTGGTTTGTGAATTGTATCTTGGGTATTCTGAGCTTCTGGGCTAATAGCCACTTATCAGTGAGTGCATACCACGTGTGTTCTTTTGTGATTGAGTTGCTTCACTCAGGATGATATTGTCTTGTTCCATCCATTTGCCTACGAATTTCATGAATTCGTTGTTTTTAACAACCGAGTAGTATTCCATTGAGTAAATGTACCACATTTTCTGTATCCATTCCTCTGTTGAGGGACATCTGGGTTCTCTCCAGCTTCTGGCTATTATAAATAAGGCTGCTATGAACATAGTGGAGCATGTGTCCTTGTTACATGTTGGAGCATCTTCTGGGTATATGCCCAGGAGTGGTATTGCTGGGTCTATATGATTTTATGATAATAGTGATAAAACCACTGTGTTGAGCTTATTAAGATTTGTGGATCATTGTGTTAGTGAAATAAGCCAGGTACAAGAAGACAAGGGTCACAGGATCTTACTCATAGGTAGAATCCCCAAAGGTTGGCCTCTTGAAGAAGTCAAGAAAGAGAGTAATGGTTACCAGAGAGGTTGGGAGAGTAGGGAGAAGGGGTGGGAGAAGCTGATTAAGGTTTAGGGGACGATGTTCAGTTAGACAGGAGCCAGGCACTCTGCCATGTATTGCAGAGGGACTGACTAGAAATACCAGTAACTACGATAGACCTCAAAAAGCCCGAGGGAAGTTTTCACTATTTCAAAAACATCAGAAATGTCCAAGGAGGTAAATATATTTAATCTGATGTAAAGATTATATAGTAATAATACATATCATTTTTATGGTTTTATATATAAGTTAAAATAACTAAAACTTAAAAACAGGAGAGCCGTTTATCATATCTGTGTATGTATATATGTCAGAGGAAAGTCATAGGGCGTATGGGATTCGTTCAGGGCCCTGCTCCCTCCTGTTTCACTGCCCTCCCATGTTAAGTACCAAAGAAGCCAGAGTCCCCAAAGCATCTCTCTGTCCAG
Seq C2 exon
GTGCCCAACAACCGGAACGTGAAGGTGCGCTTCAAACTCTTCTATCTGGTGGACCCCAACGTACCAGTGGGCTCCTGCACCAAGGACTATGTGGAGATCAACGGGGAGAA
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000031995-St14:NM_011176:9
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:
PF0043115=CUB=PU(29.5=93.9)
A:
NA
C2:
PF0043115=CUB=FE(34.3=100)


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:
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
  • Muscular differentiation time course
  • Spermatogenesis cell types
  • Reprogramming of fibroblasts to iPSCs
  • Hematopoietic precursors and cell types