DreEX6038636 @ danRer10
Exon Skipping
Gene
ENSDARG00000086819 | scn1a
Description
sodium channel, voltage-gated, type I, alpha [Source:ZFIN;Acc:ZDB-GENE-040426-751]
Coordinates
chr9:50259642-50267419:-
Coord C1 exon
chr9:50267356-50267419
Coord A exon
chr9:50264625-50264766
Coord C2 exon
chr9:50259642-50259848
Length
142 bp
Sequences
Splice sites
3' ss Seq
GCCACATGTGTGCATTTCAGGCA
3' ss Score
7.51
5' ss Seq
CAGGTGTGT
5' ss Score
6.99
Exon sequences
Seq C1 exon
GTAATCAATATTTCCTACCAGGAAAAAAAGATGCACTGATCTGTGGAAATTCTTCTGATGCTGG
Seq A exon
GCAGTGTCCAGAGGGATATACGTGTTTAAAAGCAGGTAACAATCCAGATTATGGTTACACAAGCTTTGATTCGTTCGGCTGGGCTTTCCTTTCCTTGTTCAGACTGATGACTCAAGACTTCTGGGAGAATCTTTACCAACAG
Seq C2 exon
ACTCTTCGGGCCGCTGGGAAAACCTATATGATTTTTTTCGTGCTGGTCATTTTCTTGGGATCCTTCTACCTGGTGAACCTCATCCTGGCTGTAGTCGCCATGGCATACGACGAACAGAATCAAGCCACGATCGACGAGGCTTTGAAAAAAGAGGAAGAGTTCAACGCCATGCTTGAGCAGATCACGAGACAGGAGCAGGAAGCTGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSDARG00000086819-'14-14,'14-13,15-14=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=0.130
Domain overlap (PFAM):
C1:
PF146251=Lustrin_cystein=PU(50.0=86.4),PF0052026=Ion_trans=PU(18.4=81.8)
A:
PF146251=Lustrin_cystein=PD(47.4=37.5),PF0052026=Ion_trans=FE(48.0=100),PF0382411=NicO=PU(17.3=47.9),PF0253517=Zip=PU(14.4=47.9),PF057587=Ycf1=PU(11.2=41.7),PF0479111=LMBR1=PU(9.0=27.1)
C2:
PF0052026=Ion_trans=PD(32.7=45.7),PF0382411=NicO=FE(51.9=100),PF0253517=Zip=FE(43.1=100),PF057587=Ycf1=FE(38.5=100),PF0479111=LMBR1=FE(47.6=100),PF0293211=Neur_chan_memb=PU(34.2=90.0),PF074236=DUF1510=PU(49.6=88.6)

Main Skipping Isoform:
NA
Other Inclusion Isoforms:
Other Skipping Isoforms:
NA
Associated events
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
AAAAAGATGCACTGATCTGTGGA
R:
CTTCCTGCTCCTGTCTCGTGA
Band lengths:
242-384
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]