Special

DreINT0009143 @ danRer10

Intron Retention

Gene
Description
dynein, axonemal, heavy chain 10 [Source:HGNC Symbol;Acc:HGNC:2941]
Coordinates
chr5:27761646-27762094:+
Coord C1 exon
chr5:27761646-27761867
Coord A exon
chr5:27761868-27761946
Coord C2 exon
chr5:27761947-27762094
Length
79 bp
Sequences
Splice sites
5' ss Seq
CAGGTGAGA
5' ss Score
9.22
3' ss Seq
AGGAACAAAAATTCTCGTAGATG
3' ss Score
0.89
Exon sequences
Seq C1 exon
CTGGATAAAGGACCTGGAGGAGCTGAAGCAGCGGCGAGTGCGTCTTCTGGGAGACTGTCTAATCTGCGCTGCCTTCCTCAGCTATGAAGGAGCCTTCAGCTGGGACTTCCGTAACGAAATGGTGTATAAGGTATGGCAGGCAGACGTCCTGGAAAGAGGCATTCCTCTGAGCCAGCCTTTCCGAATAGAAAACCTGCTCACTGATGAGGTGGAGATCAGCAG
Seq A exon
GTGAGACATCAACCCATCTGTGGAACATTTAATGTTACTGTATATAACTGCATTTACGGAGGAACAAAAATTCTCGTAG
Seq C2 exon
ATGGGGATCTGAAGGTCTCCCTCCAGATGAGCTCTCAGTGCAGAACGGCATCCTGACTACCAGATCTAGCCGCTTCCCCTTGTGCATTGACCCCCAGCAGCAAGCGCTTAACTGGGTCAAAAAAAAGGAGGAGAAGAACAATCTGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSDARG00000061486:ENSDART00000135878:52
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:
PF127772=MT=PD(14.5=65.3),PF127812=AAA_9=PU(3.9=12.0)
A:
NA
C2:
PF127812=AAA_9=FE(21.2=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:
TAAGGTATGGCAGGCAGACGT
R:
GGGAAGCGGCTAGATCTGGTA
Band lengths:
174-253
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]