Special

HsaINT0046147 @ hg38

Intron Retention

Gene
Description
DEAD-box helicase 31 [Source:HGNC Symbol;Acc:HGNC:16715]
Coordinates
chr9:132648189-132648551:-
Coord C1 exon
chr9:132648432-132648551
Coord A exon
chr9:132648296-132648431
Coord C2 exon
chr9:132648189-132648295
Length
136 bp
Sequences
Splice sites
5' ss Seq
CAGGTGAGC
5' ss Score
9.6
3' ss Seq
TTTTTTTTTTACAATCACAGAAT
3' ss Score
7.38
Exon sequences
Seq C1 exon
ACTCCGCAAAGGAATAAATATCCTTATCTCAACTCCTGGACGCCTGGTGGATCATATAAAATCCACAAAGAACATTCATTTTAGTCGGCTGCGGTGGTTGGTGTTTGATGAAGCAGACAG
Seq A exon
GTGAGCCTCGTCCCAGGATGATAACAGGTAGAAGAGAAGGGCTGTTTCTCCTCTCCTTGTTGCAACTTCTGTAGCCCCTTAGACCACATCTGCTCTTCATATAGTTGAAAATTTCTTTTTTTTTTTACAATCACAG
Seq C2 exon
AATCTTGGATTTGGGTTTTGAAAAGGACATCACAGTGATACTTAATGCTGTAAATGCTGAATGCCAAAAACGACAGAATGTCTTGCTATCAGCGACACTCACAGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000125485:ENST00000372159:10
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(22.5=100)
A:
NA
C2:
PF0027024=DEAD=FE(20.2=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CCGCAAAGGAATAAATATCCTTATCT
R:
CTGTGAGTGTCGCTGATAGCA
Band lengths:
221-357
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains
  • Pre-implantation embryo development