Special

RnoINT0162869 @ rn6

Intron Retention

Gene
Description
villin 1 [Source:RGD Symbol;Acc:1307048]
Coordinates
chr9:81701532-81701863:+
Coord C1 exon
chr9:81701532-81701610
Coord A exon
chr9:81701611-81701764
Coord C2 exon
chr9:81701765-81701863
Length
154 bp
Sequences
Splice sites
5' ss Seq
GAGGTGAGA
5' ss Score
7.66
3' ss Seq
TTTTTCTCTATTGGCTCTAGGAC
3' ss Score
9.79
Exon sequences
Seq C1 exon
TGTGTCTGATTCAGAAGGAAAAATGGTGGTTAGAGAAGTTGCTACTCAGCCACTCACACAGGACTTGCTCAGCCATGAG
Seq A exon
GTGAGAGGGTCTGGAGGACCCCAAGCAAGGGACACCTATAAAATGCTAATTTATCTGCAGATTTAGTGGAGGTAAACCTGGCACAGCCTTACCTCTCCCCTTCCCCCAACCCCAGCACCACAGGGTCAATTTTTTTTTTCTCTATTGGCTCTAG
Seq C2 exon
GACTGTTACATCCTGGACCAGGGAGGCCTGAAGATCTTTGTGTGGAAGGGAAAAAATGCCAATGCCCAGGAGAGGAGCGGAGCCATGAACCAGGCTTTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000015408:ENSRNOT00000021432:8
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.111 A=NA C2=0.030
Domain overlap (PFAM):

C1:
PF0062617=Gelsolin=PU(21.8=63.0)
A:
NA
C2:
PF0062617=Gelsolin=FE(41.0=100)


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:
TGTGTCTGATTCAGAAGGAAAAATGG
R:
CAAAGCCTGGTTCATGGCTCC
Band lengths:
178-332
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]