Special

BtaINT0029707 @ bosTau6

Intron Retention

Gene
ENSBTAG00000012485 | C9orf114
Description
chromosome 9 open reading frame 114 [Source:HGNC Symbol;Acc:HGNC:26933]
Coordinates
chr11:99321702-99322107:-
Coord C1 exon
chr11:99322058-99322107
Coord A exon
chr11:99321833-99322057
Coord C2 exon
chr11:99321702-99321832
Length
225 bp
Sequences
Splice sites
5' ss Seq
CAGGTAAGG
5' ss Score
11.08
3' ss Seq
TGGCCCCTCTACAACCGCAGGGC
3' ss Score
7.5
Exon sequences
Seq C1 exon
GTACCTAAGAAAGGCCTTCTTCCCCAAGCATCAGGATCTGCAGTTTGCAG
Seq A exon
GTAAGGCTGGGGGAGGGGACCTGACCCCCATTTCGCATGGATCCTCCTCCAGGCCCTGAGAACTCATGGTCCAGTTGGGAGAGCAAGACCTGTGCCTCATGGCACACTGAGCTGGATCCTGGACCAGCGTTCCCAACCTCATCACCCACCCACCTGCCCCACCCCCCGCCACCCCCGTGCGCCTCTGCACCTCCCAGATTCTTCCTGGCCCCTCTACAACCGCAG
Seq C2 exon
GGCTCCTGAACCCCTTGGACAGCCCTCACCACATGCGTCAAGATGAGGAATCTGAGTTCCGAGAGGGTGTTGTGGTGGACCGGCCCACCCGGCCTGGCCAGGGCTCCTTTGTCAACTGTGGCATGAAGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000012485:ENSBTAT00000016565:6
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.432
Domain overlap (PFAM):

C1:
PF0259812=Methyltrn_RNA_3=FE(5.8=100)
A:
NA
C2:
PF0259812=Methyltrn_RNA_3=FE(14.7=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
CCTAAGAAAGGCCTTCTTCCCC
R:
TCATGCCACAGTTGACAAAGGA
Band lengths:
173-398
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Pre-implantation embryo development