Special

HsaEX6063352 @ hg19

Exon Skipping

Gene
ENSG00000198917 | C9orf114
Description
chromosome 9 open reading frame 114 [Source:HGNC Symbol;Acc:26933]
Coordinates
chr9:131589311-131591434:-
Coord C1 exon
chr9:131591389-131591434
Coord A exon
chr9:131591014-131591139
Coord C2 exon
chr9:131589311-131589470
Length
126 bp
Sequences
Splice sites
3' ss Seq
TAGGATGTTCTTTTATCCAGAGA
3' ss Score
4.44
5' ss Seq
GCGGTGAGC
5' ss Score
8.02
Exon sequences
Seq C1 exon
GGTGAACACGGCCAAAGGATTGAGTGGCGAAAATGGAAGCAACAGA
Seq A exon
AGAAAGAGGAGAAAAAAAAATGGAAGGATCTCAAGCTGATGAAAAAACTGGAGCGGCAGCGGGCACAGGAGGAACAGGCAAAGCGCCTGGAAGAGGAGGAGGCAGCGGCAGAGAAGGAGGACCGCG
Seq C2 exon
GGCGGCCCTACACACTGAGCGTAGCCCTGCCGGGCTCCATCCTGGACAATGCTCAGTCGCCGGAGCTTCGCACCTACTTGGCCGGTCAGATTGCCAGAGCCTGTGCCATCTTCTGTGTGGATGAGATCGTGGTGTTTGATGAGGAGGGCCAGGATGCCAA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000198917-'1-5,'1-2,3-5=AN
Average complexity
A_S
Mappability confidence:
100%=100=100%
Protein Impact

Alternative protein isoforms (Ref)

No structure available
Features
Disorder rate (Iupred):
  C1=0.750 A=0.674 C2=0.037
Domain overlap (PFAM):

C1:
NO
A:
NO
C2:
PF0259812=Methyltrn_RNA_3=PU(16.8=90.7)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GGTGAACACGGCCAAAGGATT
R:
CATCCTGGCCCTCCTCATCAA
Band lengths:
202-328
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains