Special

RnoINT0047758 @ rn6

Intron Retention

Gene
Description
disco-interacting protein 2 homolog B [Source:RGD Symbol;Acc:1305671]
Coordinates
chr7:141870169-141871612:+
Coord C1 exon
chr7:141870169-141870226
Coord A exon
chr7:141870227-141871537
Coord C2 exon
chr7:141871538-141871612
Length
1311 bp
Sequences
Splice sites
5' ss Seq
AAGGTATTC
5' ss Score
6.8
3' ss Seq
ATTTCCTCTTTGATTCTCAGATC
3' ss Score
9.57
Exon sequences
Seq C1 exon
GGTCCGTCTTGTGGAACGAGGTGCCCCCCAGAGTCTCCTGCTTTCTGAGTCTGGAAAG
Seq A exon
GTATTCTGTTCTGCTAGCTGCTGGGGAAGGCTGGGATGGAGGAAGAGGACTGAAGCCTGAGGGTAGAGTCCAGTAAAGCTTGGGGAGAAGCCCACAGGTTTCCCTTAGCGGATGGTTTCAGATGCATGAAGCCAGATGTGGACTTATCTCTCTATTGTTTAAACCCCATAGACATGCCATTCCTGCTGATAAGCCAGCAAAGTGAATAGAGAAGCAGCACCTGAGGAGAGCCAGCTCTGTCTGTAAACACTGAGAGTCAGGATGGAGAGGAGGGTGGGCTGGGGGGAGAGCTTGCACCCACGGGGCAGCAGCAGCGGCAGCGGCAGCGGCGGCAGCAGCATTGCCTATGGAGTGAGCAGCTGCTCTGGGCATCCATTTATCCCATCCCTCTGTCCTCATCACCTCCCCCTCCACTATCCCTCACCCTGACCTGCCCAGACAAAGGACAGAATTATGAAGATGTCTCAGGGTCCTGCCTAGGGATCCTGAGGCAGAGGAGAAAGAAAACCCAAAGGAGCCCCTGCCTACTCTCTCCAGCGGATGTCACAACACAGGGGCTTGTGTGGAAATGCTTGTGTGGGCCATGCCATTCAGTGCTCATGTCTGCAGCTGGGTGCACATGGAAGCCGGAATGTCAGGTCATGAGGGAGGCCATCGCTGCCCTTTATTTACTTCCTCTAGGTTTAGATATTTAAACCGATACACTAGGCAAGTGGCTTACTGCTGAACTACACTGCTGACCCAGGAAACATGTTTGGTGAGCCCTGATCCGTGGGCCCAGACAGCACATAGGTTTCTTTTCCCTTCTGGAAGATCCTGGAGATGTGCCATCTCTCTCAGGGATGTGTTTCTGTGTTCGCACTAAATGCATTACCCACTGCAGCCGAGCTCCCTGTGGAGTGGTCTCCAGGTGTCTCCTCCTGCTGCTCATCTTTGGAAAGACTTACCCAAAAGGGAATGGCTGAGTTATTTACCAAAGTCTTGCAGTTGTGGCCTTGAGCAAAAGTTTCTCATCCCTCTGAAGAGATGGCAGTCTAGGTCAGTGTTCTAGCTTCAGAGTGGAATTCATTGGTCCTCCATCTCTACTACGATGAGGAAGGTTGACCAGGAACAAACAGAAAAACACCTTAGGACCCTTTGCGAGATGACTGCTTCATCAGCTCCTGCCATTTCTAGTCCAGTTCCTAGAGGTCATTGGTTGATTGCAGGGTTTGGGGTTGGAAGCCATGCCTCAGACCAGTAAACTAAGCCACAGCCAAAGTTATGCAGTTTGGTTAAACTGAGTATTTGTATTTCCTCTTTGATTCTCAG
Seq C2 exon
ATCTTACCTGGAGTGAAAGTAGTTATTGTGAATCCTGAGACCAAAGGACCTGTTGGAGACTCTCACCTGGGAGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000056106:ENSRNOT00000086577:34
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=0.080
Domain overlap (PFAM):

C1:
PF0050123=AMP-binding=FE(4.0=100)
A:
NA
C2:
PF0050123=AMP-binding=FE(5.0=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:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]