Special

RnoINT0102282 @ rn6

Intron Retention

Gene
Description
notch 3 [Source:RGD Symbol;Acc:620761]
Coordinates
chr7:14166216-14166672:-
Coord C1 exon
chr7:14166415-14166672
Coord A exon
chr7:14166335-14166414
Coord C2 exon
chr7:14166216-14166334
Length
80 bp
Sequences
Splice sites
5' ss Seq
CAGGTGCGT
5' ss Score
9.73
3' ss Seq
TCCTGCATCTGTTTGTTCAGGGC
3' ss Score
7.58
Exon sequences
Seq C1 exon
GAGTTCTCTGTGAGATCAATGAGGATGACTGTGGCCCAGGCCCATCCTTGGACTCAGGCCTCCGGTGCCTACACAACGGCACCTGTGTGGACCTGGTGGGTGGCTTCCGCTGTAACTGTCCCCCAGGGTACACAGGTCTGCACTGTGAGGCGGACATCAATGAGTGCCGACCCGGCACCTGTCATGCAGCACATACCCGGGACTGCCTACAAGATCCAGGTGGGCACTTCCGCTGCATCTGTCTCCCTGGCTTCACAG
Seq A exon
GTGCGTATGATGGAGAGGCTGGCCAGGGCGCCGACGTGGTCCTACCGTTGCAGTTGACCCTCCTGCATCTGTTTGTTCAG
Seq C2 exon
GGCCTCGATGTCAGACTGCTCTGTTCCCCTGTGAGTCCCAACCGTGTCAGCATGGAGGCCAGTGCCGTCCCAGCCTAGGCCGTGGAGGTGGGCTGACCTTCACCTGTCACTGTGTCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000004346:ENSRNOT00000037456:22
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:
PF0000822=EGF=PD(17.1=6.9),PF0000822=EGF=WD(100=43.7),PF126612=hEGF=PU(69.2=10.3)
A:
NA
C2:
PF126612=hEGF=PD(23.1=7.5),PF0000822=EGF=PU(80.6=72.5)


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:
ATACCCGGGACTGCCTACAAG
R:
CAGTGACAGGTGAAGGTCAGC
Band lengths:
178-258
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]