Special

DreINT0055028 @ danRer10

Intron Retention

Gene
Description
ddb1 and cul4 associated factor 17 [Source:ZFIN;Acc:ZDB-GENE-071008-1]
Coordinates
chr9:3537005-3537624:-
Coord C1 exon
chr9:3537519-3537624
Coord A exon
chr9:3537148-3537518
Coord C2 exon
chr9:3537005-3537147
Length
371 bp
Sequences
Splice sites
5' ss Seq
ATGGTGGGT
5' ss Score
6.18
3' ss Seq
TTCAATGCTTCTCTCCACAGAGT
3' ss Score
11.02
Exon sequences
Seq C1 exon
TTTAGAACTGAGGAGCTGATTCTGGGACAGCAGTGTGAGCTGAATAATGCAAGGGGAATCGTGGGAGATGCTCCATATGGTGTTCCGGTCAACATTTGCATTCATG
Seq A exon
GTGGGTGACGGAGTCATTCCAGAAGTATGGATGCAGTCCTCCAAGCTCATGATGGAGTCAGACACAATATTCATTCTGTCTCCACTGCAGCAGGACTTTATATTCTATACTGGACATTATTTCTGTTCAGTGATGAGACTTTAGTCTAAGCGAAGTCAGACCTTACAGTCCTAATTAAATCATTAGAAATCAAGGCATGATCATGTTTTATTTTGGTCTAATAAGCGTCATCTAGAGGCTTTTGCCTTTCATGTAAGCCACCATTGATATCAATTGATCAACTATAAGTCTAGGTATTACTTGTTGTTCCTAAAACTTCAAGTTTAGTACAATATTTCAGCAAATATTGGTTTCAATGCTTCTCTCCACAG
Seq C2 exon
AGTGTCCCCCAGTCTTGTTTGAGATGACATACTTTGAGAATGGGGTTCAGATTGGAGGACATCCTTGGCACTACATCTACACCCCCAACCACAAGAGACACAGAGGAACCCACCACGTCTGCTCCATCACAGATGGAGCTCTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSDARG00000074909:ENSDART00000145043:8
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:
NO
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
AGAACTGAGGAGCTGATTCTGG
R:
CATCTGTGATGGAGCAGACGT
Band lengths:
238-609
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]