Special

GgaEX0022522 @ galGal3

Exon Skipping

Gene
ENSGALG00000015358 | Q91377_CHICK
Description
NA
Coordinates
chr1:90785470-90789056:-
Coord C1 exon
chr1:90788707-90789056
Coord A exon
chr1:90787840-90787964
Coord C2 exon
chr1:90785470-90785585
Length
125 bp
Sequences
Splice sites
3' ss Seq
TTATTATTTGTTTGTTTCAGAGG
3' ss Score
10.01
5' ss Seq
GAGGTAAGG
5' ss Score
10.28
Exon sequences
Seq C1 exon
AAAAAAGCTTGCTGCCCGCCTGCAAGAAGCTGAGGAAGCAATTGAAGCTGCCAACGCCAAGTGCTCTTCTCTGGAAAAGACAAAGCACAGGCTGCAGAACGAGCTGGAAGATATGATGATTGATCTGGAAAAGGCCAACTCAGCGGCTGCCTCCCTGGACAAGAAGCAGCGTGGCTTTGACAAGATCATCAATGACTGGAAGCAGAAGTATGAAGAGTCACAGGCTGAGCTGGAAGCTTCCCAGAAGGAGGCCCGCAGCCTCAGCACCGAGCTCTTCAAGCTGAAGAATGCCTATGAAGAGACACTGGACCATCTGGAGACTCTGAAACGGGAAAACAAGAACCTCCAAG
Seq A exon
AGGAAATTTCTGATCTGACCAATCAGATCAGTGAAGGAAACAAGAACCTCCATGAGATAGAAAAAGTCAAGAAGCAGGTAGAACAAGAAAAGTCAGAGGTTCAGCTAGCTCTGGAAGAAGCAGAG
Seq C2 exon
GGAGCTTTGGAGCATGAAGAAAGCAAGACCCTTCGTTTTCAGCTTGAGCTTTCTCAGCTTAAAGCTGATTTTGAAAGGAAGCTGGCAGAAAAGGATGAAGAAATGGAAAATATAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000015358-'36-36,'36-35,37-36
Average complexity
S
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.508 A=0.905 C2=0.590
Domain overlap (PFAM):

C1:
PF0157614=Myosin_tail_1=FE(13.6=100),PF0003816=Filament=FE(38.9=100),PF131661=AAA_13=PD(52.9=84.7),PF078897=DUF1664=PD(79.5=52.5),PF045827=Reo_sigmaC=PU(62.8=87.3)
A:
PF0157614=Myosin_tail_1=FE(4.8=100),PF0003816=Filament=FE(13.6=100),PF045827=Reo_sigmaC=FE(25.0=100)
C2:
PF0157614=Myosin_tail_1=FE(4.4=100),PF0003816=Filament=PD(10.0=76.9),PF045827=Reo_sigmaC=PD(11.0=46.2)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
CTCCCTGGACAAGAAGCAGC
R:
GCTGAAAACGAAGGGTCTTGC
Band lengths:
243-368
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]