Special

RnoINT0105358 @ rn6

Intron Retention

Gene
Description
olfactory receptor 292 [Source:RGD Symbol;Acc:1333185]
Coordinates
chr1:212806225-212806936:+
Coord C1 exon
chr1:212806225-212806542
Coord A exon
chr1:212806543-212806621
Coord C2 exon
chr1:212806622-212806936
Length
79 bp
Sequences
Splice sites
5' ss Seq
CGGGTGAGT
5' ss Score
9.89
3' ss Seq
CTGACTGGGTTTCTCCACAGGGA
3' ss Score
10.04
Exon sequences
Seq C1 exon
GTCTCCAGGATGCCCTGCGGCTAAGGGATGGAGAGAGCTACTGTGATGGCCGAGTGGAGGTCTTCCTGGATGGCACATGGGGGCGTGTGCTGGACAATGCCTGGGACCTGCGTGATGCTGCTGTGGTGTGCAGACAGCTCGGGTGCGGAGAGGCACAGCTAGCCTATGACTCACCAGCACCGGGTTATAAGGCAATTCCTGTGGGGCTGAGCCTGGTGCACTGCTTGGGCACTGAGACCCACCTGACCCAGTGCAATGTTTCGGCTTCTTTGCTGGTCCAGGCAGGGACGTTGCGGGATGCAGGCGTGGTGTGCTCGG
Seq A exon
GTGAGTGTGGGGTGTCCACTTGCCCCTACCCCAGCCTTGTTCATGTAGTCCAATGTGTTCTGACTGGGTTTCTCCACAG
Seq C2 exon
GGAGCTTACGCATACGGTTGGCAGCGGGCAAGAGCCGCTGTGCTGGGCGTGTGGAAGTGTTCTATCAGGGCTCATGGGGCACCGTATGTGATGATGCCTGGGACCTGCAGGATGCCCATGTCGTGTGCAGGCAGCTGGGCTGTGGCCATGCCCTCAGTGCCCCCAGGGCTGCCCATTTTGGAGCAGGAACTGGGCACATCTGGTTGGATGAACTGGGCTGCCTGGGTGAGGAGGCTGCTCTATGGGAGTGCCAGTCAGGAGGTTGGGGCAAACAAGACTGTGGACACAAGGAGGACGCAGGTGTGATCTGTTCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000036647:ENSRNOT00000025680:6
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=0.000
Domain overlap (PFAM):

C1:
PF0053013=SRCR=WD(100=91.6)
A:
NA
C2:
PF0053013=SRCR=WD(100=92.5)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
Human
(hg38)
No conservation detected
Mouse
(mm10)
No conservation detected
Mouse
(mm9)
No conservation detected
Chicken
(galGal4)
Zebrafish
(danRer10)
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
CACCTGACCCAGTGCAATGTT
R:
CCCAGGCATCATCACATACGG
Band lengths:
181-260
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]