Special

MmuINT0097610 @ mm10

Intron Retention

Gene
Description
multiple EGF-like-domains 10 [Source:MGI Symbol;Acc:MGI:2685177]
Coordinates
chr18:57275681-57277123:+
Coord C1 exon
chr18:57275681-57275827
Coord A exon
chr18:57275828-57276988
Coord C2 exon
chr18:57276989-57277123
Length
1161 bp
Sequences
Splice sites
5' ss Seq
GAAGTAAGT
5' ss Score
9.82
3' ss Seq
CTATGAGTTTCTATTTGCAGTCT
3' ss Score
6.32
Exon sequences
Seq C1 exon
GTGTGCACTGTGACAGTGTGTGCGCTGAGGGACGCTGGGGTCCTAACTGCTCGCTGCCCTGCTACTGTAAAAATGGGGCTTCGTGTTCTCCGGATGATGGCATCTGTGAGTGTGCACCCGGATTCCGAGGCACCACTTGCCAGAGAA
Seq A exon
GTAAGTGTCTCCTACATGATGCTTTCTGCCCCCACCCCTCGTGTCCCCTTTCCTGGGAATTATGTACAGAATCATCTCTGCCCCACCCCTTAGTTCCTAGTGACATTTTGAGGCAGCTGAGGGAAGAGTCCTTGAAGAACTGTCCTCAAATAACACTTCCCCAAGAATTTTACCCTTTCCAACCTCCAGAACCAACTTAACAGATGGGGGCGTTAACCCTTTCTTCTTAGTGACTATTTCTTTACCTCATTGGCATGATCATCAGGACACGTTTCTCAATTCCTCCTTGGAGTGCCCAAATGGTGTTCCAGAAATCCACTGACCTGTAAATATTTTATTCGGCAATTTGGCATCAGCCTCACCTCAATTACCAGAAGCCAACATCAGCCAAACCTTGAGGCAATCACACACCTCCCTTAGTAAGCTGAAAGTCAGCGCCCTGGGGAAAGCAGAATTGAAAGTTAAAAATGGAGACCACTGATGTTGCTCCGTAGGAACCTCGAACAAAGACATGATCTGCAACAGTTCACTAAATCTTTCAGTGCATGTAACCAAGAAAGAATATGTAACTGGTTATAACATGCACTGTTGTAATTTCTCAAATCAGCTGATTTTTTCCATTAAAGAGTTCTATGCCATCATTCTATATTTAAAACCAAATAAAGCCTTTGGAAGTACCCAGATCCATAGCGTTCTGTTCCTCACCCACTCTAATCTAATCACAGGCATTCACCTGTACTTTTTTTTTAAGAAGAAATATCTTCAAACCTCATGTGTCTATCGTTTTTTGCCAATCTTGATTCTTGAAGAATAATGGATCATTCAACAATAACTCAGCAATGCTTAATTGAGATACTGATATTTAGAGTTTCATTTTCCCCATTTCCTTATTTGTTCTACAAAACGTCTTCGAGCCCCTGGTCTAGGGCTGGCCTTGAGTCAACCGCTGGAAGATAGTGGTATACGGAAGACATCCCCTCACCCCAGGGAAATCTGGACTCTAGTGGCTTCTTCCCTTGTTAAAAGCTGCCTTCTTGTTTCATGCCTGAAAAGTCCCTATTACCGGTTAGAGTTTTCTTATTCCCCCAGTTTCAGTAAACCTCTGTGTGGAGCAGGAGATAAACCCAACTTGGGGAAGTAACTATGAGTTTCTATTTGCAG
Seq C2 exon
TCTGCTCCCCCGGTTTTTATGGACATCGCTGTAGCCAGACCTGCCCGCAGTGTGTGCACAGCAGTGGGCCCTGCCACCACATCACGGGCCTGTGTGACTGCTTACCTGGCTTCACCGGTGCCCTGTGCAATGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000024593:ENSMUST00000075770:14
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=0.000
Domain overlap (PFAM):

C1:
PF126612=hEGF=PD(23.1=6.0)
A:
NA
C2:
PF126612=hEGF=WD(100=28.3)


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:
ACTGTGACAGTGTGTGCGC
R:
GCACCGGTGAAGCCAGGTAA
Band lengths:
262-1423
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