Special

MmuINT0172931 @ mm9

Intron Retention

Gene
Description
villin 1 [Source:MGI Symbol;Acc:MGI:98930]
Coordinates
chr1:74466369-74468029:+
Coord C1 exon
chr1:74466369-74466479
Coord A exon
chr1:74466480-74467826
Coord C2 exon
chr1:74467827-74468029
Length
1347 bp
Sequences
Splice sites
5' ss Seq
CGGGTAACC
5' ss Score
5.26
3' ss Seq
CATCTGTGCCCTCTCTACAGGGC
3' ss Score
11.17
Exon sequences
Seq C1 exon
GTGGAAATGTCCTGGAAGAGTTTCAACAGAGGGGATGTCTTCCTGCTGGACCTTGGGAAGCTTATTATCCAGTGGAATGGGCCAGAGAGTAACCGCATGGAGAGACTTCGG
Seq A exon
GTAACCCCATCAGGGCACCTCATTTCTGCAATTCAACATGCCTCATCGGCTTCACTCGTCTCAGTGTCACCTACCCTAGTCAACCTCAACCCCACAGCCCCGCAACTACCCCACCCCACAGGCTTCTCTCTGGCACTTCTGGGGACAGGACAGTGTGTGAAAGTAGACCTAAGTCTCTATGTACATGAAGAGGCATACTGCTTGTGTGTACTTGTGGCTAACCCTTACGGTAGAATATGTCTCCGTAGTATGGCAAGCCCCATTCTCAGCCTTGGGTATTCAGGAGGATGAGGTGGGCAGAGCTTTGCCCTGGCTCTACCCAGAAGCCGGCCGACTGGTCAAAAAAACGTAAGGGAAAGGATGAATCAGAGAACTGGAGAAGTTCGGTACTAGGCATACAGGGAGACTTTGGGGATCAGATGGAGGTGAGGCAAAGGCCCTGGGGCAGGAAAGTAGCTGGTATTGCCCAGTAGGAAGATGCTGAGCAGGTAGCAGGTCTCATCGGCAGGATGTGCGCCCAACAGGTTGTGAGTTAGGTCCTTACTGGGTACACCCAGCTAATGAAGCTTATCTGATCTCTAAGTGGAAATGGGCTGCGAAGGGGACCAGGTGGAATCCCAGCTTAACTATGTATGGGGTGAAGATGCAAAGCCTTATGCTTGAGAACAGTAGGGAAGAGTAGCGGCCCAGTTCCTGAGATGGGGAGAACCTCTAGGGGGGAAACAGAGGGCACTTTTGACTATCTGAAGAGGCTCTGTCCTACGATGAGAGCCGAGAGCTAGGCTGGAGACAGAAGCACACAGCTGTTGCTGTCCACAGGGCCCAGGGACTCCAGATGGCTCACGAAGGGAGTGGTCTTGGGCTGAAAAAGTGAACCACAGTGTGTGTACACATGAAAGCTGTCACTCTCCGGACTATGTGTGCAGATACATGCCTGTGTGAACTTTCATGGAACCGAACTATGTGTGTGTCTAAGTATTTGTGTATAGATATGTTCATGTGAATTTGCATCTGCACCGTGAGCATGTGTACCTTGGGCAGACTAAGTAGAGTACTATGACCTTTGAGGTTCAGCTCTTGTACAGAAGGGAAGCCATAAATTCCCAACAATGTCAAAACTACAGGCACAGCTAGACCATCGCAAACACACCTCCGCCCCCAACCATCACCTACGAGGAGATCTACCTCCCCATAGCTTCCAACCGTTGCCTCACACACCTGAAAAGCCTTGTTTCCACCTCTTGTAGATCTGCACAATGGGGTGGAGTTTGCCCAGCAAAGTTCAGGGTGGTGAACACTGCTACCCTGTCTGCCAACCTTCATGGGTCATCTGTGCCCTCTCTACAG
Seq C2 exon
GGCATGGCCTTGGCCAAAGAGATCCGAGACCAGGAACGGGGTGGACGTACCTACGTAGGTGTGGTGGACGGGGAGAAGGAAGGGGACTCCCCACAGCTGATGGCAATTATGAACCACGTGCTGGGCCCACGCAAAGAACTGAAGGCTGCTATTTCTGACTCAGTGGTGGAGCCGGCCGCTAAGGCTGCACTCAAGCTGTACCA
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000026175-Vil1:NM_009509:6
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.081 A=NA C2=0.143
Domain overlap (PFAM):

C1:
PF0062617=Gelsolin=FE(48.0=100)
A:
NA
C2:
PF0062617=Gelsolin=PD(40.0=44.1)


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:
GTGGAAATGTCCTGGAAGAGT
R:
GTACAGCTTGAGTGCAGCCTT
Band lengths:
312-1659
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