Special

DreINT0009127 @ danRer10

Intron Retention

Gene
Description
dynein, axonemal, heavy chain 10 [Source:HGNC Symbol;Acc:HGNC:2941]
Coordinates
chr5:27749041-27749702:+
Coord C1 exon
chr5:27749041-27749301
Coord A exon
chr5:27749302-27749529
Coord C2 exon
chr5:27749530-27749702
Length
228 bp
Sequences
Splice sites
5' ss Seq
AAGGTGCAA
5' ss Score
2.22
3' ss Seq
ATGTCTATTTTATTTTATAGCCC
3' ss Score
8.93
Exon sequences
Seq C1 exon
GTGGATGAATATGGAACTCAACAACCTATAGCTCTCCTCAAGCTTCTGTTGGACAGGGGTGGCATGTATGACCGAGGAAAAGAACTCAACTATAAACTCATAAAGGACCTGGGCTTCATTGCAGCCATGGGGAAGGCAGGCGGTGGTAGGAATGAAGTGGACCCACGATTCATCTCTCTTTTCAGTGTGTTCAACATCCCCTTCCCTGAGGAGGAATCCCTACATCTCATCTACTCTTCTATTCTAAGAGGACACACCAAG
Seq A exon
GTGCAAGAGATATTTCAGCTTCTTGATTAAAAAATGATGGGATGTGCTGACATGAAGTCAAATATTAAATATAGGTGTCTATTGTAGGGCTGCACTGATGGAATGAGATATTTCTTCATTGCAATTATTTTCTCATGTTGTGTTTATAATTTAGATTTTCGTATAAATATTTATCTTGATTCTATTTTATGATTTTTAAATCAGAATTATGTCTATTTTATTTTATAG
Seq C2 exon
CCCTTTGAGGAGTGCATCCGAAACATCTGTGACAAGCTGACGTTTTGCACTCTGGAGCTGTACAAAACCATAATTAAGGATTTACCGCCAACACCTTCCAAGTTCCACTACATCTTTAACCTGAGAGATCTCTCCAGAGTCTACCATGGCCTGACGCTGACCAACCCTGAGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSDARG00000061486:ENSDART00000135878:38
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:
PF127752=AAA_7=FE(31.6=100)
A:
NA
C2:
PF127752=AAA_7=FE(21.0=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:
TTCATTGCAGCCATGGGGAAG
R:
CAGGCCATGGTAGACTCTGGA
Band lengths:
300-528
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]