HsaEX0011630 @ hg19
Exon Skipping
Gene
ENSG00000148362 | C9orf142
Description
chromosome 9 open reading frame 142 [Source:HGNC Symbol;Acc:27849]
Coordinates
chr9:139886870-139887426:+
Coord C1 exon
chr9:139886870-139887014
Coord A exon
chr9:139887092-139887152
Coord C2 exon
chr9:139887377-139887426
Length
61 bp
Sequences
Splice sites
3' ss Seq
TGACAGGCCTTCTCCCCCAGCGT
3' ss Score
5.49
5' ss Seq
CTCGTGGGT
5' ss Score
1.88
Exon sequences
Seq C1 exon
CGCCGGGTTCCCGCTCGCCCGGCGCCATGGATCCGCTGTCGCCGCCGCTCTGCACGCTGCCGCCGGGCCCCGAGCCGCCCCGCTTCGTGTGCTACTGCGAAGGGGAGGAAAGCGGGGAGGGGGACCGCGGCGGCTTCAACCTCTA
Seq A exon
CGTGACCGACGCCGCGGAGCTTTGGAGCACCTGCTTCACGCCGGACAGCCTGGCGGCCCTC
Seq C2 exon
AAAGCCCGTTTTGGCCTGAGTGCGGCTGAGGACATCACCCCCCGGTTCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000148362-'0-3,'0-0,1-3
Average complexity
S
Mappability confidence:
100%=100=100%
Protein Impact
ORF disruption upon sequence exclusion
Show structural model
Features
Disorder rate (Iupred):
C1=0.350 A=0.000 C2=0.000
Domain overlap (PFAM):
C1:
PF153841=DUF4610=PU(17.2=85.0)
A:
PF153841=DUF4610=FE(10.1=100)
C2:
PF153841=DUF4610=FE(8.1=100)
Main Skipping Isoform:
NA
Other Inclusion Isoforms:
NA
Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Chicken
(galGal3)
No conservation detected
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
CATGGATCCGCTGTCGCC
R:
GCACTCAGGCCAAAACGGG
Band lengths:
143-204
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
SPECIAL DATASETS
- The Cancer Genome Atlas (TCGA)
- Genotype-Tissue Expression Project (GTEx)
- Autistic and control brains
- Pre-implantation embryo development
Other AS DBs:
FasterDB (Includes CLIP-seq data)
AS-ALPS (AS-induced ALteration of Protein Structure, links to PINs)
APPRIS (Selection of principal isoform)
DEU primates (Only for human)