Special

BtaINT0050793 @ bosTau6

Intron Retention

Gene
Description
dynein, axonemal, heavy chain 9 [Source:HGNC Symbol;Acc:HGNC:2953]
Coordinates
chr19:31046964-31047558:+
Coord C1 exon
chr19:31046964-31047094
Coord A exon
chr19:31047095-31047431
Coord C2 exon
chr19:31047432-31047558
Length
337 bp
Sequences
Splice sites
5' ss Seq
CAGGTGATG
5' ss Score
5.99
3' ss Seq
GAAATTCTTTGTGCCCTCAGGCT
3' ss Score
7.61
Exon sequences
Seq C1 exon
GATTCTAAAAGATTTGAAGGCATCGACATAGACTTTAAAGAGTTAGCTTATGATGCTCGGAAAACGCCAAATGTAGTGGAAGCCACCAACAAGCCAGGTCTTTACGAAAAGCTGGAAGATATTCAGAGCAG
Seq A exon
GTGATGGCCGGTGTGCAGTTGCCTTTGTAATGGAGAGGCTTTGTCTCTCTTTGTCTCTCAAGTCCTTACCTTAGTTAACTGCCCGAGTGAGAGAGTGAACATGTGTATCTGGTCGGGTACCTTGATTTGCCTGTGTGCTTGGGTAACATGGGATATTGTTAGAGGTGTTTATTCTGATTGAAATGTACTAGTAGGGCTATATGCACATGCCCACAGATGTTCCATGTATACATCACTCCTGAGGATAATCCACAAGTCACACTCGTTTGCATTTAGGTAACAGCCACATGCCTCTGGATCCTGGCAAACCTAACAAGGAAATTCTTTGTGCCCTCAG
Seq C2 exon
GCTGTGCCTGTGTGAGAAGGCCCTGGTGGAGTACCTGGACACAAAAAGGCTTGCCTTCCCCAGGTTTTACTTCCTCTCCTCTTCTGATCTTCTAGACATTCTTTCCAATGGCACAGCCCCTCAACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000022509:ENSBTAT00000006131:21
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:
PF083938=DHC_N2=FE(10.4=100)
A:
NA
C2:
PF083938=DHC_N2=FE(10.1=100)


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:
TTCTAAAAGATTTGAAGGCATCGACA
R:
GCTGTGCCATTGGAAAGAATGT
Band lengths:
246-583
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Pre-implantation embryo development