Special

RnoEX0060454 @ rn6

Exon Skipping

Gene
Description
notch 1 [Source:RGD Symbol;Acc:3187]
Coordinates
chr3:3921118-3923630:-
Coord C1 exon
chr3:3923517-3923630
Coord A exon
chr3:3921553-3921672
Coord C2 exon
chr3:3921118-3921270
Length
120 bp
Sequences
Splice sites
3' ss Seq
CTACGTATCTTTCTTTCTAGGAG
3' ss Score
10.13
5' ss Seq
AAGGTGAGG
5' ss Score
9.16
Exon sequences
Seq C1 exon
GCCCTAACTGCCAGACCAACATTAACGAATGTGCTTCCAACCCCTGCCTGAACCAGGGCACCTGCATTGATGATGTCGCTGGGTACAAATGCAACTGCCCTCTGCCCTATACAG
Seq A exon
GAGCCACATGTGAGGTGGTGTTGGCCCCATGTGCCACCAGCCCCTGCAAAAACAGTGGGGTATGCAAGGAGTCTGAGGACTATGAGAGCTTTTCCTGTGTCTGTCCCACAGGCTGGCAAG
Seq C2 exon
GTCAAACCTGCGAGATCGACATCAATGAGTGTGTGAAAAGCCCGTGTCGCCATGGTGCCTCTTGCCAGAACACCAATGGCAGCTACCGCTGCCTCTGCCAGGCTGGCTACACGGGTCGCAACTGCGAGAGTGACATCGATGACTGCCGACCCA
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000019322-'18-18,'18-17,19-18
Average complexity
S
Mappability confidence:
100%=100=100%
Protein Impact

Alternative protein isoforms (Ref)

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

C1:
PF0000822=EGF=PD(6.5=5.1),PF0000822=EGF=PU(90.3=71.8)
A:
PF0000822=EGF=PD(6.5=4.9),PF0000822=EGF=PU(90.9=73.2)
C2:
PF0000822=EGF=PD(6.1=3.8),PF0764510=EGF_CA=WD(100=73.1),PF0000822=EGF=PU(9.7=5.8)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TAACGAATGTGCTTCCAACCCC
R:
GTCGGCAGTCATCGATGTCAC
Band lengths:
242-362
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]