Special

MmuINT0172929 @ mm9

Intron Retention

Gene
Description
villin 1 [Source:MGI Symbol;Acc:MGI:98930]
Coordinates
chr1:74464934-74466251:+
Coord C1 exon
chr1:74464934-74465130
Coord A exon
chr1:74465131-74466142
Coord C2 exon
chr1:74466143-74466251
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-Vil1:NM_009509:4
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.030 A=NA C2=0.027
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
  • Muscular differentiation time course
  • Spermatogenesis cell types
  • Reprogramming of fibroblasts to iPSCs
  • Hematopoietic precursors and cell types