Special

RnoINT0046008 @ rn6

Intron Retention

Gene
Description
DEAD-box helicase 31 [Source:RGD Symbol;Acc:1304895]
Coordinates
chr3:7437340-7438782:+
Coord C1 exon
chr3:7437340-7437384
Coord A exon
chr3:7437385-7438740
Coord C2 exon
chr3:7438741-7438782
Length
1356 bp
Sequences
Splice sites
5' ss Seq
GAGGTAAGT
5' ss Score
11.08
3' ss Seq
CAACTTTTTCATACTTACAGTTG
3' ss Score
7.32
Exon sequences
Seq C1 exon
CGTAGTGATGGCCCCTATGCTTTGGTCCTAGTGCCCACCAGAGAG
Seq A exon
GTAAGTAAGCAGATACTTGTAGGTGAGGTTTGTGCGCACTGTAAGTGATGGTGGCCTGTTGACTTGAAGCACTTTCTTCACTTCCCTGCAGACGAATCTCTGCCCCTGCTTTTCTTCACATGCCTTCTCAGGACCTGTCCTGCGGGGTTTGTTAAGGAGGAATGGTTAAGTGCTCTTTAAAAATCACGGGCTGGGTACGAGAAGACATTTCTCCGTTGTCTAATAAAAGACTAACAATACTTAGATTGCTAATCCTTTAAAATAAATTAGAGGAATTGCATTTTTATGCTTCCAAGTATCTTAAAGAATGTGACTGAAAAATTTGGATCTAAAAATGAACCTTGTTGTTCATGGAAGTAAATAGAAATAGCTTCTGTCAGATCTGGGTGATGCATCCTCAAAGAACTTTCAGGAAAATGGAAATTTCCAGACAGCTTTGCTTTCTTTGTTTCTGACTTTGTTTTCTTTTAAGATTTATTTTTATTTAATGTGTTTGGGTGTTTTGCCTATGTGTATGTCTGTGAACCATATGTGTACAGTGTCCATGGATACCAGAAGAGGGTGTCAGTCTTGGAAGTGAAGTTAGAACCAACTGTGAGCTGATATGTGGGTGCTGGGAACCGAACCTGGGTTCTCTGCGAGAGCAGCCAGTGCTCTTGACTGCTAAGCTCTGTCCAGCCTCTCTGGTCTGCCTTTCATACAGTCTGCTCTCTACTCTGTGTCTGTTCTGTCCAGGGAGGAGCATGAGCGGGGAGGCACGTTGAAATGTTTTCGGCAGCAAACCTGTCACTTCTCTAGAATGTTAATCATTGTAGGGACAGCACACAACTATGGACACCATTCTGTAGGACTGTTTTGATAGTGTTTAGTAGTTACCACCTAGATTAATTTTACTATTCCTAAATCCATTGGGCTTCTCTTTGTAAACTCAGGACTGACCCTGTGCACCTGAGAATACAGCCAAGTTCCCCAGTACCTGTCAGGCTGCTGCTGTGCTCTCCCTCTAATGCACAATACGCTTCCTTTCTGTGGAGAGCCAAGACCAGTTGACATCTTTTCATTTTCTTCCAAGCCTACACTGAACTTCTCTGTGTGACACTGGGAGTCTGAGCCAGCAGAGGGAGCACAGAACACTGTTTTTCTATGTCTAAGAATGTATGTGATATCTTCACTCTCAGTTCCTAAACTGACAGATTTCAAACCAGTCTTAAGAAGAGATCTCTGTAGAGCATTTACTTGTCCTAAGCCTTGAGGTCCAGGGCTGTACCCTGATCGATTCAGACGGTCTTTTCTTTACAAATGTAAAAAGGAAGCAAGGGGCCCTGCTTACTGTCTCCAACTTTTTCATACTTACAG
Seq C2 exon
TTGGCTCTGCAAAGCTTTGACACTGTTCAGAAGCTACTTAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000013040:ENSRNOT00000064323:7
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:
PF0027024=DEAD=FE(7.9=100)
A:
NA
C2:
PF0027024=DEAD=FE(7.3=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
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]