Special

DreINT0009145 @ danRer10

Intron Retention

Gene
Description
dynein, axonemal, heavy chain 10 [Source:HGNC Symbol;Acc:HGNC:2941]
Coordinates
chr5:27762185-27762908:+
Coord C1 exon
chr5:27762185-27762464
Coord A exon
chr5:27762465-27762678
Coord C2 exon
chr5:27762679-27762908
Length
214 bp
Sequences
Splice sites
5' ss Seq
CCGGTGAGA
5' ss Score
8.72
3' ss Seq
TTTAATTTTTTTGTTTTTAGTTA
3' ss Score
8.49
Exon sequences
Seq C1 exon
ATCTCATCATTCAATGATCCAGACTTCTTGAAGGGGTTGGAGTTGGCTATTAAGTATGGATTCCCCTTCCTCTTCCAAGATGTGGATGAATATATCGATCCCGTAATTGACAACGTTCTTGAGAAGAATATAAAAGGGGCAGAGGGGCGCCAGGTTGTCGTACTTGGTGATAAGGAAGTTGACTACGATCCCAACTTCAAACTTTACCTCAATACCAAACTTGCAAACCCAAAGTTCTTACCTGCAGTATTTGGGAAGGCTATGGTTATCAATTACACCG
Seq A exon
GTGAGAGCAAACACTATGCAGTATACACCAGTTGATGCTTATTAACAGCAAGTATTGATGTAAGAACTGTACAACAATCGGAATTTATCACACTAAATTTAAAAACTGTTATTTGTTTTTAAATAACACACTTCGATTTTTTTCTGACTTTAGTGTTAATATGCATTTAATTTGGGATTTTACAGATTTTTTTGTTTAATTTTTTTGTTTTTAG
Seq C2 exon
TTACCCTGAAGGGATTGGAAGATCAGCTGCTGAGTGTTATTGTAGGATTTGAGCGAAAGGAGCTGGAGGAGCAAAGAGAAAGGCTTATTCTAGAGACTAGTGAGAACAAACGCTTGCTGAAAGATCTGGAGGACTCACTGCTGAGAGAGCTGGCCACCTCTACTGGAAACATGCTGGATAATGTTGAGCTCATACAGACTCTGGATGAAACCAAGTCCAAAGCCAACGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSDARG00000061486:ENSDART00000135878:54
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=0.013
Domain overlap (PFAM):

C1:
PF127812=AAA_9=FE(40.3=100)
A:
NA
C2:
PF127812=AAA_9=FE(32.9=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:
GCCAGGTTGTCGTACTTGGTG
R:
TGTTTCCAGTAGAGGTGGCCA
Band lengths:
303-517
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]