MmuEX0007744 @ mm10
Exon Skipping
Gene
ENSMUSG00000063145 | Bbs5
Description
Bardet-Biedl syndrome 5 (human) [Source:MGI Symbol;Acc:MGI:1919819]
Coordinates
chr2:69654063-69655634:+
Coord C1 exon
chr2:69654063-69654112
Coord A exon
chr2:69654246-69654373
Coord C2 exon
chr2:69655499-69655634
Length
128 bp
Sequences
Splice sites
3' ss Seq
TAATAAATTTGACTTTACAGAAA
3' ss Score
7.03
5' ss Seq
CAGGTACAA
5' ss Score
7.09
Exon sequences
Seq C1 exon
CTATTGGTTACAACTGCATATTGAATATCACAACAAGAACTGCTAACTCT
Seq A exon
AAACTGCGAGGCCAAACCGAAGCTCTTTATATATTGACAAAATGCAACACTACCCGGTTTGAGTTTATATTCACAAACCTGGTTCCCGGGAGCCCCAGACTTTTTACTTCTGTGATCGCAGTGCACAG
Seq C2 exon
AGCATATGAAACTTCTAAAATGTACCGTGACTTTAAGTTGAGAAGTGCAGTCATTCAGAACAAGCAGCTGAGGTTACTACCACAGGAGCATGTGTATGATAAGATCAATGGCGTATGGAATCTGTCCAGCGACCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000063145_MULTIEX1-2/2=1-C2
Average complexity
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:
PF072896=DUF1448=FE(19.3=100)
A:
PF072896=DUF1448=FE(12.5=100)
C2:
PF072896=DUF1448=FE(13.4=100)
Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TGGTTACAACTGCATATTGAATATCA
R:
CTGGTCGCTGGACAGATTCC
Band lengths:
182-310
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
SPECIAL DATASETS
- Pre-implantation embryo development
- Ribosome-engaged transcriptomes of neuronal types
- Neural differentiation time course
- Muscular differentiation time course
- Spermatogenesis cell types
- Reprogramming of fibroblasts to iPSCs
- Hematopoietic precursors and cell types