MmuEX0043138 @ mm10
Exon Skipping
Gene
ENSMUSG00000017664 | Slc35c2
Description
solute carrier family 35, member C2 [Source:MGI Symbol;Acc:MGI:2385166]
Coordinates
chr2:165278241-165281380:-
Coord C1 exon
chr2:165281308-165281380
Coord A exon
chr2:165280786-165280954
Coord C2 exon
chr2:165278241-165278416
Length
169 bp
Sequences
Splice sites
3' ss Seq
CTGTACTGTCCCCCCTGTAGCGT
3' ss Score
9.51
5' ss Seq
TTGGTGAGC
5' ss Score
7.43
Exon sequences
Seq C1 exon
GTACACGATGACCAAATCCTCTGCTGTGCTCTTTATCCTGATTTTCTCTCTCATCTTCAAGCTGGAGGAACTG
Seq A exon
CGTGCAGCCCTGGTCCTGGTGGTCCTGCTCATTGCTGGGGGCCTCTTCATGTTTACCTATAAGTCCACGCAGTTCAATGTGGAGGGCTTTGCCTTGGTGCTGGGGGCTTCGTTCATCGGTGGCATCCGCTGGACCCTTACACAAATACTCCTGCAGAAAGCCGATCTTG
Seq C2 exon
GTCTCCACTTGTCCACCTCTGAGAAGATCTTCCGCTTCCAGGACACAGGGCTGCTCCTGTGGGTGCTTGGGAGCCTCCTCCTCGGTGGGATTCTGGCCTTCGGTTTGGGCTTCTCCGAGTTCCTCCTGGTCTCCAGAACGTCAAGCCTCACACTCTCCATCGCTGGCATCTTTAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSMUSG00000017664_MULTIEX1-3/5=2-C2
Average complexity
C3*
Mappability confidence:
100%=100=100%
Protein Impact
ORF disruption upon sequence inclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.000 A=0.000 C2=0.000
Domain overlap (PFAM):
C1:
PF084496=UAA=FE(16.2=100)
A:
PF084496=UAA=PD(29.3=89.5),PF0315111=TPT=WD(100=47.4)
C2:
PF0315111=TPT=FE(38.4=100)
Main Skipping Isoform:
NA
Other Inclusion Isoforms:
Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
ACACGATGACCAAATCCTCTGC
R:
AAAGATGCCAGCGATGGAGAG
Band lengths:
244-413
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