Special

RnoEX0021210 @ rn6

Exon Skipping

Gene
Description
cholinergic receptor nicotinic alpha 6 subunit [Source:RGD Symbol;Acc:69281]
Coordinates
chr16:68862027-68865369:+
Coord C1 exon
chr16:68862027-68862166
Coord A exon
chr16:68864172-68864281
Coord C2 exon
chr16:68864394-68865369
Length
110 bp
Sequences
Splice sites
3' ss Seq
GACCCCTCTATTTCTTTTAGGTC
3' ss Score
10.7
5' ss Seq
TAAGTATGT
5' ss Score
4.58
Exon sequences
Seq C1 exon
GCAGTAGAGGCTGTGTGTCTGAGGAACAGCTCTTCCACACACTCTTCGCCCACTACAACCGCTTCATCCGGCCAGTGGAAAACGTTTCTGATCCCGTCACGGTGCACTTTGAGTTGGCCATCACGCAGCTGGCCAATGTG
Seq A exon
GTCTGGAAGGACTACAGATTGTGTTGGGATCCAACGGAGTACGATGGCATCGAGACGCTTCGTGTTCCAGCAGATAACATCTGGAAGCCTGACATCGTTCTGTATAATAA
Seq C2 exon
TGCCGTCGGCGACTTCCAGGTCGAAGGCAAGACCAAAGCTCTTCTTAAGTACGATGGGGTGATAACCTGGACCCCGCCAGCCATCTTTAAGAGTTCCTGTCCAATGGACATCACCTTCTTCCCATTTGATCATCAAAACTGCTCCCTGAAATTTGGGTCCTGGACTTACGACAAGGCTGAAATCGACCTTCTCATCATTGGCTCTAAAGTGGACATGAACGACTTTTGGGAAAACAGTGAGTGGGAAATTGTCGATGCCTCTGGCTACAAGCATGACATCAAGTACAACTGCTGTGAAGAGATTTACACAGATATCACCTACTCGTTCTACATCAGGAGACTGCCCATGTTTTATACCATCAATCTCATCATCCCCTGCCTCTTCATTTCCTTTCTCACCGTGCTGGTCTTTTACCTTCCTTCCGACTGTGGCGAGAAAGTGACTCTTTGCATCTCGGTTCTGCTTTCTCTAACTGTCTTTTTGCTGGTGATTACAGAGA
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000012283_MULTIEX1-2/3=C1-3
Average complexity
C2
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=0.104
Domain overlap (PFAM):

C1:
PF0293118=Neur_chan_LBD=PU(18.8=83.0)
A:
PF0293118=Neur_chan_LBD=FE(17.4=100)
C2:
PF0293118=Neur_chan_LBD=PD(55.6=35.3),PF103294=DUF2417=WD(100=51.5),PF0293211=Neur_chan_memb=PU(86.0=62.3)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
AACGTTTCTGATCCCGTCACG
R:
GGTCGATTTCAGCCTTGTCGT
Band lengths:
248-358
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]