Special

RnoINT0049196 @ rn6

Intron Retention

Gene
Description
dynein, axonemal, heavy chain 8 [Source:RGD Symbol;Acc:619986]
Coordinates
chr20:9428315-9428929:+
Coord C1 exon
chr20:9428315-9428561
Coord A exon
chr20:9428562-9428687
Coord C2 exon
chr20:9428688-9428929
Length
126 bp
Sequences
Splice sites
5' ss Seq
AGGGTAGGC
5' ss Score
7.26
3' ss Seq
CCATGCATCCTTGTTTTCAGGTG
3' ss Score
9.25
Exon sequences
Seq C1 exon
TTATATGAGACCTCTCTGGTACGGCACGGCCTGATGACCCTCGGGCCAAACAGTTCCGGGAAGACGACGGTCATAACAATTCTGATGAAGTCATTAACGGAGTGCGGGAGGCCCCACAGAGAGATGCGAATGAACCCAAAGGCGATTACCGCGCCTCAGATGTTCGGCCGGCTGGACACAGCCACCAACGACTGGACAGATGGGATCTTCTCCACCCTGTGGAGGAAGACATTAAAAGCTAAAAAGG
Seq A exon
GTAGGCAGGGACGCCCCTCCCAGTCTGCCCTTTCTCTGCAAGCTTATTAACAACGGGAGAGCATTTGCTTGCTCCTTTTTTCTGATGGAGAAACCGATCCATCTTCCCATGCATCCTTGTTTTCAG
Seq C2 exon
GTGAAAACATCTTCCTCATCTTAGATGGCCCCGTGGATGCCATTTGGATCGAAAACCTAAACTCTGTGCTAGACGACAACAAGACACTCACCCTGGCCAATGGGGACCGCATTCCCATGGCCCCGACCTGTAAGCTGCTGTTTGAGGTGCACAACATTGAGAACGCGTCCCCCGCCACGGTGTCGAGGATGGGTATGGTGTACATCAGCAGTTCGGCTCTCAGCTGGAGGCCGATATTACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000000542:ENSRNOT00000000651:61
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.108 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF077289=AAA_5=PU(53.3=88.0)
A:
NA
C2:
PF077289=AAA_5=PD(46.0=77.8)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
CGGGAAGACGACGGTCATAAC
R:
TCGATCCAAATGGCATCCACG
Band lengths:
243-369
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]