BtaEX6087194 @ bosTau6
Exon Skipping
Gene
ENSBTAG00000007090 | MYH2
Description
Bos taurus myosin, heavy chain 2, skeletal muscle, adult (MYH2), mRNA. [Source:RefSeq mRNA;Acc:NM_001166227]
Coordinates
chr19:30144281-30146691:-
Coord C1 exon
chr19:30146302-30146691
Coord A exon
chr19:30145076-30145202
Coord C2 exon
chr19:30144281-30144399
Length
127 bp
Sequences
Splice sites
3' ss Seq
TTCCACTTTTCCTCTCACAGGGA
3' ss Score
10.63
5' ss Seq
CTGGTAACT
5' ss Score
5.45
Exon sequences
Seq C1 exon
GCCCGCATCGAGGAGCTGGAGGAGGAGATCGAGGCCGAGCGGGCCTCCCGCGCCAAGGCAGAGAAGCAGCGCTCAGACCTCTCCCGGGAACTGGAGGAGATCAGCGAGCGGCTAGAAGAAGCCGGCGGGGCCACTTCCGCCCAGATTGAGATGAACAAGAAGCGGGAGGCCGAGTTCCAGAAGATGCGCAGGGACCTGGAGGAGGCCACCCTGCAGCACGAGGCCACGGCGGCCGCTCTTCGCAAGAAGCACGCGGACAGTGTGGCTGAGCTGGGGGAGCAGATTGACAACCTGCAGAGGGTCAAGCAGAAGCTGGAGAAGGAGAAGAGCGAGATGAAGATGGAGATCGACGACCTTGCTAGCAATGTGGAAACGATCTCTAAAGCCAAG
Seq A exon
GGAAACCTAGAGAAGATGTGCCGAACTCTGGAGGACCAAGTGAACGAGCTGAAATCCAAGGAGGAGGAGCAGCAGCGGCTGATCAATGACCTGACAACCCAGAGGGGACGCTTGCAGACTGAATCTG
Seq C2 exon
GTGAATTTTCACGTCAGCTAGATGAGAAAGAAGCTCTGGTGTCTCAGTTGTCAAGGGGCAAACAAGCATTTACTCAACAGATTGAGGAATTAAAGAGGCAACTTGAAGAGGAGATAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000007090-'28-35,'28-34,29-35=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=0.892 A=0.953 C2=0.175
Domain overlap (PFAM):
C1:
PF0003816=Filament=FE(45.4=100),PF0157614=Myosin_tail_1=FE(15.0=100)
A:
PF0003816=Filament=FE(14.8=100),PF0157614=Myosin_tail_1=FE(4.9=100)
C2:
PF0003816=Filament=PD(4.2=30.0),PF0157614=Myosin_tail_1=FE(4.5=100),PF0003816=Filament=PU(11.8=87.5)
Main Skipping Isoform:
NA
Other Inclusion Isoforms:
NA
Other Skipping Isoforms:
NA
Associated events
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
CTGGAGGAGGCCACCCTG
R:
GCCCCTTGACAACTGAGACAC
Band lengths:
254-381
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]