Special

BtaINT0050833 @ bosTau6

Intron Retention

Gene
Description
dynein, axonemal, heavy chain 9 [Source:HGNC Symbol;Acc:HGNC:2953]
Coordinates
chr19:31185398-31188684:+
Coord C1 exon
chr19:31185398-31185586
Coord A exon
chr19:31185587-31188448
Coord C2 exon
chr19:31188449-31188684
Length
2862 bp
Sequences
Splice sites
5' ss Seq
CAGGTGTGT
5' ss Score
6.99
3' ss Seq
TGCCCTTTCTTTCCCACCAGGTT
3' ss Score
12.95
Exon sequences
Seq C1 exon
GTGGGAGGCCTGGCCTCTGAAAACGTGAGATGGGCAGAAGCTGTGCAGAACCTCAAGCAACAGGAAAGGAAATTATGTGGAGACATTTTACTCACTGCAGCTTCCATCTCGTACCTGGGCTTCTTTACAAAGCGGTACCGCCAGAGCCTCCTAGACGCGGCGTGGAGGCCCTACCTGAGCCAGCTGCAG
Seq A exon
GTGTGTCTGGCCCACGTCACTCGTGAGCTCACGTGACAGTAGCAATACAAATCTTCTAGTCCCTTCCTGCGTTCTTCCTCCCGTCACCTCCAGAGCATCCCCTAGTGACCTCCGGGATCCAGGACGGAGACCTGGGCACCCATGTCCTTCCACACTTCCATGTACCGCCATGCACTGCCCTCCAGGTCACCTGGGGACAGCACCTGTCCTCCTTCTGGGGTCTGCGTGGGAACTCTGGCCCACCACCTCCATGCTGTCTCCTGACTGTTCTCAAAACTGTTAAACCCACGAGGCACCAAACACATCCTGTATTTCCCTCCAACCTTCCTGCTCTTGTGCCAAACTTAATAGCAGCAGTGGAGGGCACACCTCCTTCCCCAAATGCTGCCCCCCTGGTTACTGTGCCCCGAGCACCACGTCTGTGTCTGTGACCTACAGACACCCCTATGAAGGCAGTTCATCGGCTTTGGTCAAACGTCCTCAGCTCTCAGTGTGAGTAGGTGGCTCACGCTGACATGACCTGATGGGGAAATGCCAGTTTCCAACCGAAGAGGACTCAGGGTGTGTTGCCCCTCGACACTCTCACAGCGCTCATGGTCCTCAACCCACAAGCACTTGCCAAGTCTTCATCCTGTCCTACATGCCACTGGCGGGAGGCACAGAAGACAGTCCGTACCAGGGTGTCGGCGGGACAGTCTTAGTCCCGCAGTCAAGACGAGAGTCATAAGAAGCAGCTGCCTGAGAGTTAGCACAGAAGAATCACCACGTACAGTTAGGGTTGTGTTCCAGAATGCATTTATAGGTGTCTCCTTGGAACACAAAGCCCAGACCGTCTAGTGATGGTTGGCTTCTCAGATCAGCTCATAAAATCCCACCCACCTGATAATTTGCTGAACAGTAGTTTAAAAACTCTTATAGTGCATTTCCCTGGTGGTCCAGTCGTTAAGACTCTGTGCTTCCAAGGCAGGGGGCACAGGTTTGATCCCTTGTTGGGGAACTAAAATCCCACATGGCACATGGCACAGCCAAAAAATTGTTTAAATTTTTTTTAATTAAAAAAAAAAAACAGTTACAGTACTGGGAAATAAACAAAAAATTAAGCTGTTATTTATTCACTTTGAACACTTGTGGAAAGGAAATCGTTGAAAGGACAGCCATTAGCTGAACAAATGAAGGCAAGGAGCGCAATAGCAGGTTAATGAGGTGTTTTCTGGCTCTGCTTTGGGGACTCAAGTATTTTTGTGCCATGGACCCTTTTGGCAGTCTGATAAAACCGATGCATTCCTTCTCACAGTAATGTTTTGTAGTATGTAAAATGGAATGAATACGATTACAAAGGAAAACGATTCTATTGAAATACATTTCTGATGCCAGGATAAGAACTTCCAGTGTCTGGTTTTCCCTTTGAGATCTGCTCGAAGGTATAGAATTGGCCGTTCGTACTCTTAGCAGATATAATTAAAGGGAAAGGAGAGGCTTTCCTGAGATAACTGGGAGGACAAACTGCAGAGAAGAGAAGGATGGAGAGGTTAATATTAATAACAGGGCACATATGTGAACCTCAAGAGTGTTCTGAAGCCAACACAAAAGGTCACATGTATTGCATAATTCCATTTATGTGAAACCTCCAGAATAGGCAAATCCACACAGACAGAGAGCAGATTAGAGGTTGTCAGACCTGGGGGTAGCCGGGAATGGGGAGTGACTGCTCGTAGAGGTGCAGTTTCCTTTTGGGGTGAAGAAAATGTTTTGGAAAGAGACAGAGCTGAGAGTTGCACAGCATTGTGAAAGACTAAATGCCGTTGATTTGTGCACTCTGAAATGGCTAAGGAATGTGACATTTACCCCAATTAAAAAAAAAAGTTTCTAATGAAAATGATTATTCTGAGAAGAATTAAATGAGCTGAAAGAGGTAAGCAGAAGAAAAGGTAGGGTTCCCAACAGGGACAGTGGACAGGTTTGCGGGACGAGGTCCTGCAAGCAGCCTTGTGTTGAGGGGGTTGGTCTGCAGCAGGAGAAAGGAGAGGGTCTGCAGTCCTTTGCGAGCTGGGCATTGGCAGCAAGTGGTGATGCCAGTGAGAGGAGAGGGTGATCGGTGTGCGCTCGTGTGGGGACTGGGACCGTGAAGCACAGAAATGCAACAGGAAATGACTCTGCTAACACGGGTAAGGAGGATGGAGACTGCTGTTAACATGCAAATGATACTTGGTTGCTCAGTCCTATCTGACTCTTTGCAACCCCATGGACTACAGCCTGCCAGGCTCCTCTGTCCATGAGATTATCCTGGTAAGAATACTGGAGTGGGTTGCCATTTCCTCCTCCAGGGGAATCTTTCTGACCCAGGGATCAAACTTGCATCTCCTATGGCTCCTGCACTGGCAGGCAGATTCTGTACCACTGAACCGAATCCACCTGCAGTGCAGGAGACAAAGAATACTCAGGTTTGATCCCTAGGTTGGGAAGATTCCCCTGGAAGAGGAAATGGCAACTCACTCCAGTATTCTTGCCTGAAAAATCCCTTGGACAAAGGAACCTGGTGGGCTAGTCCGAAGGGTTGCAAAGAGTCAGACATGACTGAGCAAACACACTTGGATTTGATCTGATTGATCTATGGTAGTCATTTGACTTAGAAAATATACCGAAGAACCTAGGATGACAAGGGTGGGATTTCTGCTGCTGTTCATCCCTCAAGAGAAAAGACTATCAGGACGCTGAGGAAACATGCTCCGCAATCACACAGCCAGGAAAACTCTCCTCAGGGGGATTTTGGTCTTGCTTTTTAGAGGAGTTCTGTCTTTTGAGTGAGCTGTGCCCCACCCCCTGCTTCCGTTCTGAGCGCCTGTGCCCTTTCTTTCCCACCAG
Seq C2 exon
GTTCCAATCCCGGTGACCCCCACCCTGGACCCCCTACGGATGCTGATGGATGATGCCGACGTGGCCACCTGGCAGAATGAGGGCCTCCCTGCAGACCGCATGTCCACGGAGAATGCCGCCATCCTCCTCAGCTGCGAGCGCTGGCCACTCATGGTGGACCCTCAGCTACAAGGCATCAAATGGATCAAGAACAAGTATGGTGAGGACCTCCGGGTCACCCAGATCGGCCAGAAGGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000022509:ENSBTAT00000006131:64
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=0.025
Domain overlap (PFAM):

C1:
PF127772=MT=PD(16.9=92.1)
A:
NA
C2:
PF127812=AAA_9=PU(28.5=82.3)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Pre-implantation embryo development