Special

RnoINT0162859 @ rn6

Intron Retention

Gene
Description
villin 1 [Source:RGD Symbol;Acc:1307048]
Coordinates
chr9:81706969-81707754:+
Coord C1 exon
chr9:81706969-81707113
Coord A exon
chr9:81707114-81707565
Coord C2 exon
chr9:81707566-81707754
Length
452 bp
Sequences
Splice sites
5' ss Seq
CAGGTAGGA
5' ss Score
9.79
3' ss Seq
GACTGTGGGGCTCTCCACAGGTC
3' ss Score
9.07
Exon sequences
Seq C1 exon
GCTGCAGGAGGAAAACCAAGTCATCACTCCTCGGCTCTTTGAGTGCTCCAACCAGACTGGGCGCTTTCTGGCCACAGAGATCTTTGACTTCACTCAGGACGACCTGGAAGAGGATGATGTGTTCCTATTGGATGTCTGGGACCAG
Seq A exon
GTAGGAGAGGAGATCTGAGGACTGCCTTTCCCTCTACCTTGGTTCCTACCATAAGAGATCCCAGGAGCTTTAGGGTAGGGAAATGCCAAGGTCTTGCAGAGGGGCATTCTGGGTGGGGCATCCTTCTTCTTTATGAAGGAAGGAGGGAGAAATAGAGGGTCATCCCACGACTTATTTCCCATAGAAGCGGGAATGTTGCCAGGCATCTTGGGCTCTGTGGCAGAGAAATGTCACATATTCACAAGCCATCTATGGAGCAGCATGGGACCAGTCTCATATGCCAGATGTAAAGTCAAGGCCAAATCAGGCCTTGCTTAAGGTCATTAGCTGAGTAGTGTCGGGTCTTCCTAGCTAGGCATCAGGGATGAGTCAAGGCAGAGCCTGAAGGCATGGAGAATGGCCAAGCCGATGACCATGCAGGAAGGACTGAGGGACTGTGGGGCTCTCCACAG
Seq C2 exon
GTCTTCTTCTGGATAGGGAAACACGCCAACGAGGAAGAGAAGAAGGCTGCAGCTACAACTGCACAGGAATACCTCAAGACCCACCCCGGAAACAGAGACCCTGAGACCCCTATCATTGTGGTGAAGCAGGGGCACGAGCCCTCCACCTTCACAGGCTGGTTCCTGGCTTGGGATCCCTTCAAGTGGAGT
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000015408:ENSRNOT00000021432:16
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.041 A=NA C2=0.365
Domain overlap (PFAM):

C1:
PF0062617=Gelsolin=PU(33.3=53.1)
A:
NA
C2:
PF0062617=Gelsolin=PD(64.1=79.4)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GCTGCAGGAGGAAAACCAAGT
R:
ACTCCACTTGAAGGGATCCCA
Band lengths:
334-786
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]