Special

DreINT0009174 @ danRer10

Intron Retention

Gene
Description
dynein, axonemal, heavy chain 11 [Source:HGNC Symbol;Acc:HGNC:2942]
Coordinates
chr16:19399670-19400124:-
Coord C1 exon
chr16:19399946-19400124
Coord A exon
chr16:19399788-19399945
Coord C2 exon
chr16:19399670-19399787
Length
158 bp
Sequences
Splice sites
5' ss Seq
CCGGTAATG
5' ss Score
6.21
3' ss Seq
TTTTTTTTTTTTTTTAACAGAAA
3' ss Score
11.03
Exon sequences
Seq C1 exon
GATGCATTCAGAGGTCTGGACAGGGATGTTGAAGGGTCTGCCAAGCGCTGGAAGAAACTGGTGGAGTCTGAGTGTCCAGAAAGAGAGCGGTTCCCTCAGGACTGGAAGACCAAGAGCCCTCTCCAGAGACTCATCATTCTAAGAGCGATCCGGCCTGACAGGATGACCTATGCTCTCCG
Seq A exon
GTAATGAGTGTGCTTCTGAGAACCATCTAAAAAACAGCCAATCTGTCGAAAACTTTACTGTAAAATAAAATGGAGTTGGCCAGGTTTGAAACACCAGGGTTTTTGGTCCTTGAATCTCATCATTCTGTTTTTTTTTTTTTTTTTTTTTTTTTTAACAG
Seq C2 exon
AAATTTTATTGAGGACAGTTTGGGACCCAAGTATGTGCACATCAGTCATATGGAGTTTGAAAAATGTTTTGAGGAGTGCAGTCCAACAACACCAGTGTTCTTCATCCTTTCTCCTGGA
VastDB Features
Vast-tools module Information
Secondary ID
ENSDARG00000094282:ENSDART00000138744:18
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.019 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0302810=Dynein_heavy=FE(9.1=100)
A:
NA
C2:
PF0302810=Dynein_heavy=FE(5.7=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
CAGGGATGTTGAAGGGTCTGC
R:
TGGTGTTGTTGGACTGCACTC
Band lengths:
253-411
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]