Special

RnoINT0028966 @ rn6

Intron Retention

Gene
Description
calpain 11 [Source:RGD Symbol;Acc:1302946]
Coordinates
chr9:17746327-17746969:+
Coord C1 exon
chr9:17746327-17746538
Coord A exon
chr9:17746539-17746929
Coord C2 exon
chr9:17746930-17746969
Length
391 bp
Sequences
Splice sites
5' ss Seq
CTGGTGAGG
5' ss Score
8.3
3' ss Seq
TTTCACTCTCTTATGCCCAGGTT
3' ss Score
7.11
Exon sequences
Seq C1 exon
TTTCAGAACCTCCAGGACATCCACCTGAAGAAAGACTTCTTTATGAAATATCGGGACCATGGCTTTTCAGAGATCTTCACCAACACGAGGGAGGTGAACAGCCATCTTCGGCTGCCCCCCGGGGAGTACGTCATTATCCCCTCCACCTTTGAGCCTCATAAAGATGCTGACTTCCTGCTTCGAGTCTTCACAGAGAAACACAGTGAGACCTG
Seq A exon
GTGAGGGGCCAGCCTCGCTCCGGCGAGGTTCCGCGCTCCGGCGAGGTTCCGCGCTCCCAAGGGGATACAGGGTGTCAGATTCTGGTCCTCCTTCACATCAACCTTATGTTATGTCATGGAAACTGAGGCATGACGATATGAGGTCTAAATATGTGAGCTACCATATGTTTCCTGGGAATTGAACTCTGGACCTCTGGGAGAGTAGTCAGTGGTCTTAACCACTGAGACATCTCTCCAGCCCCTCTAAATTAGTAGTAGAAATAGGAATGAAACCAGGGCCCAGATTTAATGTATTATTAGATACTGCTCCACATACAATGACAGGACCCTCCCCAGATCACCTTAAGTCTCTGACCTCGTTACCCCTAAGCTTTCACTCTCTTATGCCCAG
Seq C2 exon
GTTGCTGGATGAAGTCAACATGCTTGAGCAACTCCAAGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000026025:ENSRNOT00000065754:13
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0106717=Calpain_III=FE(44.3=100)
A:
NA
C2:
PF0106717=Calpain_III=PD(0.1=0.0)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TCAGAACCTCCAGGACATCCA
R:
GCTCAAGCATGTTGACTTCATCC
Band lengths:
239-630
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]