Special

HsaEX0011749 @ hg19

Exon Skipping

Gene
ENSG00000165698 | C9orf9
Description
chromosome 9 open reading frame 9 [Source:HGNC Symbol;Acc:1367]
Coordinates
chr9:135759298-135763824:+
Coord C1 exon
chr9:135759298-135759478
Coord A exon
chr9:135762756-135762958
Coord C2 exon
chr9:135763677-135763824
Length
203 bp
Sequences
Splice sites
3' ss Seq
TGTGGCGGCGGCCCTTGCAGGTG
3' ss Score
7.68
5' ss Seq
AAAGTAAGT
5' ss Score
9.72
Exon sequences
Seq C1 exon
ATTCCTCTTCTCCTGTAAATGACCACAGAGGAAGACAATGAATGAGGTGAAAGAATCCCTTCGCAGCATCGAGCAGAAGTACAAGCTCTTCCAGCAGCAGCAGCTCACCTTCACCGCCGCTCTGGAGCACTGCAGGGAGAACGCCCACGACAAGATCCGGCCCATCTCCAGCATTGGACAG
Seq A exon
GTGCAGAGCTACATGGAACACTACTGCAACAGCTCCACAGACCGGCGGGTTCTGCTCATGTTCCTGGACATCTGTTCAGAGCTGAATAAGCTCTGCCAGCACTTTGAGGCCGTGCACTCTGGCACCCCAGTCACCAACAACCTCCTGGAGAAATGCAAAACCCTCGTTAGCCAAAGCAACGACTTAAGCAGCCTCAGAGCAAA
Seq C2 exon
ATACCCTCATGATGTGGTGAACCACCTCAGCTGTGACGAGGCCCGGAACCACTACGGCGGCGTGGTCAGCCTCATCCCCCTCATCCTAGACTTAATGAAAGAATGGATCGCCCACTCCGAGAAGTTGCCGCGCAAGGTGCTGCAGCAC
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000165698_CASSETTE1
Average complexity
S
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

Show structural model
Features
Disorder rate (Iupred):
  C1=0.000 A=0.000 C2=0.272
Domain overlap (PFAM):

C1:
PF151201=DUF4561=PU(27.3=97.9)
A:
PF151201=DUF4561=FE(39.0=100)
C2:
PF151201=DUF4561=PD(32.6=51.9)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Zebrafish
(danRer10)
HIGH PSI
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
TCTCCTGTAAATGACCACAGAGGA
R:
AACTTCTCGGAGTGGGCGATC
Band lengths:
299-502
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