Special

HsaINT0025315 @ hg19

Intron Retention

Gene
ENSG00000198917 | C9orf114
Description
chromosome 9 open reading frame 114 [Source:HGNC Symbol;Acc:26933]
Coordinates
chr9:131587050-131587328:-
Coord C1 exon
chr9:131587256-131587328
Coord A exon
chr9:131587149-131587255
Coord C2 exon
chr9:131587050-131587148
Length
107 bp
Sequences
Splice sites
5' ss Seq
CAGGTATCT
5' ss Score
7.33
3' ss Seq
AGACTCTGTTACCCCTCCAGACT
3' ss Score
6.48
Exon sequences
Seq C1 exon
GAGGTGAAGATTGACAAGAACCTGGAGCCCGGGCTTCGGGTGACTGTGCGACTGAACCAGCAGCAGCACCCAG
Seq A exon
GTATCTGGAAGGTTCCCCAACCCCTGGGTTGGCCTGATGAGCTCCAGGGTTCAGCCACCTGCTTCCATTCCCTCACCCCATCTTTACAGACTCTGTTACCCCTCCAG
Seq C2 exon
ACTGCAAGACCTACCATGGCAAAGTGGTATCATCGCAGGACCCTCGCACCAAAGCTGGTCTCTACTGGGGCTACACCGTCCGACTGGCTTCCTGCCTCA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000198917-C9orf114:NM_016390:8
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.060 A=NA C2=0.191
Domain overlap (PFAM):

C1:
PF0259812=Methyltrn_RNA_3=FE(8.2=100)
A:
NA
C2:
PF0259812=Methyltrn_RNA_3=PU(24.6=94.4)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
AGGTGAAGATTGACAAGAACCTGG
R:
GAAGCCAGTCGGACGGTGTAG
Band lengths:
163-270
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains
  • Pre-implantation embryo development