Special

RnoINT0107707 @ rn6

Intron Retention

Gene
Description
paired box 6 [Source:RGD Symbol;Acc:3258]
Coordinates
chr3:95723683-95724110:+
Coord C1 exon
chr3:95723683-95723765
Coord A exon
chr3:95723766-95723959
Coord C2 exon
chr3:95723960-95724110
Length
194 bp
Sequences
Splice sites
5' ss Seq
CAGGTACCT
5' ss Score
8.16
3' ss Seq
CCTGTTCCATGCATTTCCAGGTG
3' ss Score
11.27
Exon sequences
Seq C1 exon
AGTTTGAGAGGACCCATTATCCAGATGTGTTTGCCCGGGAAAGACTAGCAGCCAAAATAGATCTACCTGAAGCAAGGATACAG
Seq A exon
GTACCTGGGGACCATGTTGGGTTTGTGTGTTGTGGGTACTTATCTTTTGCCTTGCCTGTATGCCAGTCATTGATATAAACAGGGTTAGCTTGCAAAGACTCCCTGGTCCTAGGGCAAGGATGGGAATGGAGGGGTTTTTGTTTGCAGCAGGGCTGGTAGCAAGCACAGGGCTAACCTGTTCCATGCATTTCCAG
Seq C2 exon
GTGTGGTTTTCTAACCGAAGGGCCAAGTGGAGAAGAGAAGAAAAACTGAGGAACCAGAGAAGACAGGCCAGCAACACCCCGAGTCACATCCCTATCAGCAGCAGTTTCAGTACCAGTGTCTACCAGCCAATTCCACAGCCCACCACACCTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000004410:ENSRNOT00000005882:8
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

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

C1:
PF0004624=Homeobox=FE(47.4=100)
A:
NA
C2:
PF0004624=Homeobox=PD(19.3=21.6)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
AGTTTGAGAGGACCCATTATCCAGA
R:
CAGGTGTGGTGGGCTGTG
Band lengths:
234-428
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]