Special

HsaINT0025312 @ hg19

Intron Retention

Gene
ENSG00000198917 | C9orf114
Description
chromosome 9 open reading frame 114 [Source:HGNC Symbol;Acc:26933]
Coordinates
chr9:131588663-131588908:-
Coord C1 exon
chr9:131588819-131588908
Coord A exon
chr9:131588713-131588818
Coord C2 exon
chr9:131588663-131588712
Length
106 bp
Sequences
Splice sites
5' ss Seq
ACAGTAAGG
5' ss Score
5.42
3' ss Seq
AGGTCAGCATTCTTTCCTAGGTA
3' ss Score
4.26
Exon sequences
Seq C1 exon
GACTGTGGAGGGGGAATTCACAGGAGTTGGGAAGAAGGGGCAGGCGTGCGTACAGCTGGCCCGGATCCTGCAGTACCTGGAGTGTCCACA
Seq A exon
GTAAGGGGGTCACTCCCCTAAGCATGAGGGAGGGGTGTGTCAAAGTGGAGACCAGGTAGGAGGCGGCTTCCCCTGGGAACATCCTGAGGTCAGCATTCTTTCCTAG
Seq C2 exon
GTACCTGAGGAAGGCGTTCTTCCCCAAGCACCAGGATCTACAGTTTGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000198917-C9orf114:NM_016390:5
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.162 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0259812=Methyltrn_RNA_3=FE(10.3=100)
A:
NA
C2:
PF0259812=Methyltrn_RNA_3=FE(5.8=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
ACTGTGGAGGGGGAATTCACA
R:
TGCAAACTGTAGATCCTGGTGC
Band lengths:
138-244
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