Special

BtaINT0050839 @ bosTau6

Intron Retention

Gene
Description
dynein, axonemal, heavy chain 9 [Source:HGNC Symbol;Acc:HGNC:2953]
Coordinates
chr19:30994211-30996611:+
Coord C1 exon
chr19:30994211-30994378
Coord A exon
chr19:30994379-30996494
Coord C2 exon
chr19:30996495-30996611
Length
2116 bp
Sequences
Splice sites
5' ss Seq
GTGGTAGGG
5' ss Score
4.2
3' ss Seq
TCCATTTGCTGTCTCTTCAGGAA
3' ss Score
9.82
Exon sequences
Seq C1 exon
GATCTTCTGAAGACAACTTCGGATTTCCACAAACTGGAAAAGCTTGAGTTCAGTGGTATCAGAGGAAGTGCCTTGAGCCAGCAGGCCCAGCAGATGTACACCGAATTTCAAGAGATGTACAGGGTCTTCTCAGACTCTTCCTACGACTGCTTGGATCTCCAGAGCGTG
Seq A exon
GTAGGGCTTGGAACGGCTACCTTGCAAGCTTTGTCTCTTTTTCAGATGCCTGCAGCCTCTAGCCTGGGTATTTACTTGCATTTCCCCTGTGCGTTTTCTTTGGCTCTGTGGTCCCCATGGTTTTATTGGCAGAGACCACAATTAATTATCTTTTGTGTCAGGAGAGAAGTCAGGGGAGGGAGTTTTCCAACTGCTGACTTCTTCGGAGTGAAGATACCCAGGGTTTCAGAGATGCTGAGATGGAGATGGGGTGATGGTGGAGGCTGCAGCCACTCTGCAGCTCCCAAAGCTTTAAGCTTTGAGCAGCACCTGCTGTGTGAAGGCCAGGCACACCCAGGCAGAATTTCATTAGTGGCCCGCAGAGGGGTAAGTGACGCAGTAGCCCAGTTTTCTGATCAGACTCTAGTTCCCTAGAGAGACCTCAGGATGAGGCAAGGGCCAACATTGCATTTTCCAGGATCAGGACACGGGAGTCCACATCCCACCTGTAGTGCAGGAGAGCTGAGACCAGTGAGTGCAAGACTGCAGGAACCAAAAAAAGCAAAAGGGTCGGTACAGAAACAGGGAATGGAGTTCCCGGGAAGGGAATGGCTGGATTACTGGAAAAGGAATTTTAGAGCATTTGAGGGAAAAGGAAAAAGCAATTAAACATCTGCTCTGAGCACCCTCCACTGTCTGCGTTCGTGCTCAGTCATCACTTGTGTCTGACTGTGGTCCCGTGCACTGTAGCCCACGAGGTTCCTCTGTCCTTGGAATTCTCCAGGCAAGAATAGTGGAGTGGGTTGCCGTTTTCTCCTCCAGTGGACCTTCCTGACCAAGGACGGAACCCGCATCTCCTGCATTGGCAGGTGGATTCTTTACCACTGAACCACCTGGGAGCCCCCTTCCATTGTCTAGGGGGATCTTAGCTGGCCAAACCCAGGAAATGGAACTTTCTAAAAGTTCCATTAGTTTAAAGTAGAAAAAAAGTTGGCTTACAAAGCAGGATCTATACTGTATGTTTTCTACCATGTGATAAAACAATACAAAACAAAATCCTGTACATAGAGAAGTGTGCTCCAATGTTAGTATGGTTGGGTTTGGGAAGTAGAGAAATACTACTGTGTTTTCCTACTTTTCTTTATCTTTTCATAAAAGTATGCATAGCTATTGTAAAGCAATAATAGATAATAATTTCACAAATTAGAGATGTTTCTCTGAAAATCAATGTTCTCTGAAAATTGCTACATTTGAAGAAAGAGCATGCTCTGTGTTGCTGAATAAAATACAGTTAATTGGGACAGGCTTATACTAAAAAAAAAAAAATTCTTTGTTGATCTGAAATTTAAATTTAACGGGCATCCTGTAATTTTATTTGCTAAATTTGGCAACCGTGGGGACAATGGCTAGCTGCTGTCTTAAGCAATTAAGTGTAGTTAGAAGAAATAGTGTATAGTTGTTAAATTAGCTTACTTTTCTCCTAATAGCCATATCAATTTGTTTACACTGAAAAGAACAGGATTTTCACTTGAGGGAGGAAGGGAAGTCGGGGGTAGTGATGAAGTAGCCCCATTGTTGGGGCTGTTGCTGCCAAGGTGGCTTTCAGGGTGGCCTGAGCTGGTGCCGCAGGTGAGAGAGAAGGGGCTGCAGGAGCTGGAAGTGGGGACACAGAAGAGAGGGACAGGGGGCCAGCCTCACCTCCGACTCTTTACCATTTTGCCTCGAGTGACTCAGACAGTAAAGAATCCACCTGCAATGCAGGAGATGTGGGTTCGATTGATCCCTGGGTCAGGAAGATCCCCTGGAGAAGGGAATGGCTAACCCGCTCTGGTATTCTTTCCTGGAGAATTCCATGAACAGAGGAGCCTGGAAGACTACAGTCCATGGGGGTCACAAAGGGTCGGACACAACTGAGTGACTAGCACATGCTAATACTAGAGAATCTAGGAGAAAAATGCTTAAATAATAGGGCAGCTATTAAATATCCCTATTTAATAGGGATAAACACTGAGGCACACCATAGTGAACTATAGAAAATCAAAATATATCCTTGGTGTGACAGATTAATAGGAAAAAGCATTCCGGGATTGTCCTTCAGAAAATCATGTTTTCTTATGTCCATTTGCTGTCTCTTCAG
Seq C2 exon
GAATTTGAAAATGACATCTCTGACTTTAATCAGAGAGTAGAAGACCTTGACAGGAGGCTGGGGACTGTCTTTATTCAGGCCTTCGATGACGCCCCTGGCTTGGAGCATGCCTTCAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000022509:ENSBTAT00000006131:7
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:
PF083857=DHC_N1=FE(9.4=100)
A:
NA
C2:
PF083857=DHC_N1=FE(6.5=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
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