Special

MmuINT0172929 @ mm10

Intron Retention

Gene
Description
villin 1 [Source:MGI Symbol;Acc:MGI:98930]
Coordinates
chr1:74418360-74419677:+
Coord C1 exon
chr1:74418360-74418556
Coord A exon
chr1:74418557-74419568
Coord C2 exon
chr1:74419569-74419677
Length
1012 bp
Sequences
Splice sites
5' ss Seq
TGTGTAGGG
5' ss Score
-2.69
3' ss Seq
AGCTTTCCTTTCTTTCCCAGGAT
3' ss Score
9.87
Exon sequences
Seq C1 exon
ATCCACAAGACCAGCAGCACTCTCTCCTATGATATCCACTACTGGATTGGCCAGGACTCGTCCCAGGATGAGCAGGGGGCAGCTGCCATCTACACCACACAGATGGATGACTACCTGAAGGGCCGGGCTGTCCAGCACCGCGAGGTTCAAGGCAACGAGAGCGAGACTTTCCGGAGCTACTTCAAGCAAGGCCTTGT
Seq A exon
GTAGGGCGGGGGACAACTGGGACTGGGGAGGACACCAAGACTGGTCATCTGAGGTGGGGACTGGAACTGGGGGCTGGGCTGAAGAGACAGGGACATTAAGGCCTGAAGTGTGAGAGACTCTGGTAGGTGGGAGGTGAGCTGGCCAGACTTTCAGAAGGAAGTCTGAGGCTCTGGGGGCTCTGGGGAGCGCACATGCCTTTTGTTAATTTTTCTCCACCTTTCCATCCCTCACCCTTATCGCTGCTGTTACTCTGACCGTGGCCCCGTTCCTCTGAGTCTACTTTGGCTGGACTTACCCCTTGGCCCCTTCTGTGACTATGGCGCGTGAATTCTGTACCTTAGCTCTTGTCTACAGGGACCGCTCAGGGCCTGATGTTCTCAGGCTATTAAAGCAAGCCACGCCCACTCAGGCTAACTGGCAGGTGGCTGTTCCCTCTTCTCTCTCCAATCAGGCCTTTCACAGTGCAAAGACCTACTTTTTCTAGACAAGTCTGAAGCTGGCTCTCCTCATGGAAACCCCAGCTCCACCACCGCAGTTTCATTTAACGTGTAGGATGGAAGCTCTCCAATCACCGATATCCCTACCTCCCCTTTCTGTGTTGTTCTCTTCTACCAGCGGTTACAGTCCAAGGTTACTCTCTGGTAGTCGAGTGGCATCTCTCCCTTCTTCCGCCTCAGCGCCTGGTCACCAGAGCCTGGCGTTATGCCCACTTTCTCCTCTCCAAATTACCATGATTATCTTGGCAGACCGCTCTGCAGGGCCAGGAACTAGGGCAAGGGATAGGAAGACATACAATGCAGGGTCAGGTGCAACAATATGCTACCCGCCAGCCAAGCCCTTGTAGGACACTGATGGTGACTTTAAGCTTAATGTTTGGAACTTCCTTTGCCCACTCAGGCTAACTGGCAGGTGGCTGTCCCAGTTGGGACCTCAGAGGGCCCAAGGAAGCTCAGGACCTTGGCACAACTCTCCCACCCAGCGCCCTTAAGTCAGCTTTCCTTTCTTTCCCAG
Seq C2 exon
GATCCGGAAAGGGGGAGTGGCTTCCGGCATGAAGCACGTAGAAACAAACTCCTGTGATGTCCAGCGACTGTTGCACGTCAAGGGCAAGAGGAATGTGCTGGCTGGAGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000026175:ENSMUST00000027366:4
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.030 A=NA C2=0.018
Domain overlap (PFAM):

C1:
PF0062617=Gelsolin=PD(68.7=86.4)
A:
NA
C2:
PF0062617=Gelsolin=PU(8.0=16.2)


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:
CACAAGACCAGCAGCACTCTC
R:
TCTCCAGCCAGCACATTCCTC
Band lengths:
302-1314
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