Special

MmuEX6051162 @ mm9

Exon Skipping

Gene
Description
otogelin-like [Source:MGI Symbol;Acc:MGI:3647600]
Coordinates
chr10:107298122-107303859:-
Coord C1 exon
chr10:107303650-107303859
Coord A exon
chr10:107299201-107299366
Coord C2 exon
chr10:107298122-107298196
Length
166 bp
Sequences
Splice sites
3' ss Seq
TGACACTTGTTTGTCCACAGCTG
3' ss Score
10.03
5' ss Seq
CATGTAAGT
5' ss Score
8.31
Exon sequences
Seq C1 exon
TTGGGTATGCAGCACACTGTGATGTCATCCACCAGGAGCTCTTTGCTCCTTGCCATGTCTACGTCAGTCCCGGGCTGTACTACCAGTTGTGTCGCCACGATGCCTGCAAATGTGGGAGCCCCTGCCTGTGTAACGCTCTCGCCCACTACGCCTACCTGTGTGGTCAGCGTGGTGTGCCCATTGATTTCAGAGCTCACATCTCCTTCTGTG
Seq A exon
CTGTGGTGTGTCAGAAGGGCATGCTGTACCACCACTGCTCGTCACTCTGCCTCCGCTCCTGCACCTCTCTCTCCTCCCCTGAGCAGTGCAAAGACGACTGTGCTGAAGGGTGCAACTGTCCTGAAGGCAAATTCTATGAAGAGACACTTAACTTTTGTGTGCCCAT
Seq C2 exon
ATATCACTGCCGGTGTCATTATAGGGGGAGCATTTACCAGCCAGGGGAGCTCATTCCAACCCCCTCAGGCTTATG
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000091455-'18-19,'18-18,19-19=AN
Average complexity
A_S
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

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

C1:
PF087426=C8=WD(100=100.0)
A:
PF087426=C8=PD(0.1=0.0),PF0182612=TIL=PU(92.9=92.9)
C2:
PF0182612=TIL=PD(5.4=11.5)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TTGGGTATGCAGCACACTGTG
R:
GGCTGGTAAATGCTCCCCCTA
Band lengths:
252-418
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]