Special

HsaEX6076024 @ hg19

Exon Skipping

Gene
ENSG00000117971 | CHRNB4
Description
cholinergic receptor, nicotinic, beta 4 (neuronal) [Source:HGNC Symbol;Acc:1964]
Coordinates
chr15:78916461-78923674:-
Coord C1 exon
chr15:78923630-78923674
Coord A exon
chr15:78923418-78923527
Coord C2 exon
chr15:78916461-78917633
Length
110 bp
Sequences
Splice sites
3' ss Seq
GGCCTTGCCTGTCTGTCCAGGAA
3' ss Score
7.72
5' ss Seq
CAAGTGAGT
5' ss Score
9.1
Exon sequences
Seq C1 exon
AATGAGCGAGAGCAGATCATGACCACCAATGTCTGGCTGAAACAG
Seq A exon
GAATGGACTGATTACCGCCTGACCTGGAACAGCTCCCGCTACGAGGGTGTGAACATCCTGAGGATCCCTGCAAAGCGCATCTGGTTGCCTGACATCGTGCTTTACAACAA
Seq C2 exon
GTCGTTGAGGACTGGAAGTACGTGGCTATGGTGGTGGACCGGCTGTTCCTGTGGGTGTTCATGTTTGTGTGCGTCCTGGGCACTGTGGGGCTCTTCCTACCGCCCCTCTTCCAGACCCATGCAGCTTCTGAGGGGCCCTACGCTGCCCAGCGTGACTGAGGGCCCCCTGGGTTGTGGGGTGAGAGGATGTGAGTGGCCGGGTGGGCACTTTGCTGCTTCTTTCTGGGTTGTGGCTGATGAGGCCCTAAGTAAATATGTGAGCATTGGCCATCAACCCCATCAAACCAGCCACAGCCGTGGAACAGGCAAGGATGGGGGCCTGGGCTGTCCTCTCTGAATGCCTTGGAGGGATCCCAGGAAGCCCCAGTAGGAGGGAGCTTCAGACAGTTCAATTCTGGCCTGTCTTCCTTCCCTGCACCGGGCAATGGGGATAAAGATGACTTCGTAGCAGCACCTACTATGCTTCAGGCATGGTGCCGGCCTGCCTCTCCATCACCATC
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000117971-'2-5,'2-2,3-5=AN
Average complexity
A_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=0.045
Domain overlap (PFAM):

C1:
PF0293118=Neur_chan_LBD=FE(13.9=100)
A:
PF0293118=Neur_chan_LBD=FE(17.5=100)
C2:
PF0293211=Neur_chan_memb=PD(12.9=58.5)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
AGCAGATCATGACCACCAATGT
R:
AAAGAAGCAGCAAAGTGCCCA
Band lengths:
257-367
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains