Special

HsaINT1011591 @ hg38

Intron Retention

Gene
Description
dynein axonemal heavy chain 9 [Source:HGNC Symbol;Acc:HGNC:2953]
Coordinates
chr17:11644631-11647198:+
Coord C1 exon
chr17:11644631-11644699
Coord A exon
chr17:11644700-11647071
Coord C2 exon
chr17:11647072-11647198
Length
2372 bp
Sequences
Splice sites
5' ss Seq
AAAGTAAGC
5' ss Score
7.31
3' ss Seq
GTTGTCTCTGACCCTTGCAGGTA
3' ss Score
10.16
Exon sequences
Seq C1 exon
TTGCATGGAATCTGCAGAAGGAAAGCGAATGCAACAAAAATATGAAGATATGCTGTCATTGCTAGAAAA
Seq A exon
GTAAGCAACTTCTGGCATTGCGTGGGTCTGCAGATTGCACAGCCTCCATGCTGCCTTTTGCAGCTCCGAGTTTGTGCAGATTCCTCAGTGGCTCCGAAGTATCACTCTATGTTTTATGTTATAACCACGATATTTGTGAGTACAGTATTTCCGGGTTGCACACACACAGGGTATCTGGGGAATTCAGCTGTATTCTGGAAATAAATACTTTTCCAGTGTAGTTTTGCTGGGAGTGTGAACTAGAGCTAGGAGTGGGGTGCTACTCATGGAACTCCGAGACGGATGTCACGGAAAATTGCAACAGCTGCTTACTCAGCAGAAAGCAACAGTGCATGCTGCACAAAGAGGCAATAAGTTTTAAAAAGTACTTCCTGCATCATTTTATTGAGAAAGCATAAGAGTGAAAATTTTATATGACTTCAAAGTTGTAACTGCTTTAAAGCTGAATAAGTCTTTCCAGGGCTTAGGGTCTAGAAACAGCCATTGTCTTGATTTCTCCTTCTGCCATTTGTTCTTTCTCCTGGTTCAGGAGGGAAGAATGGTGGCCGTTGAGATTATAATTGTGATTATGCTTAGCATTGTTCCAGACAGATTAATTAACAGCACCTCTACCTGGCAAGTAACACACATTCCACCCCTTTTACCTCTAAAATAACTTCAAGTCCATCCACTCCTCTTTGTCTCCACCACCAGTGTCTTCACAAGAGACTGGAACTTCTCCAGGCTGAACTGCTGCAGTGGCTTCCTAACAGTCCTTGCTGCCTCCAGATCTGTTCCCCTCAGTACCCACATTGTTACCAAATCCAATAATGTCACCATAGCCACCACCAGCTGGGAGGCCTTGCGGTGGTTCTCACAGCCTCCTTAACATGACATGAAAAGTCTTCCTTGAGGTGGTTTTTGCCTCCTCGTCACCACCTCCAGCCTCTGCCATGCTCTGTAGTCCTTGTTTCAAGCACACAGTTTCAAGCATGCTGTTTCTCACCTCTACCCTTTGGCTACACCAGGAATGCTCACTCTCCCTTTGCCACCCAACCTCTGGCCATCCTCTGAGACCCAAGCAAGCATCCCTTCATCACCTCTCCTATGAAACCTTCCCTGACATTCTCCTTATCATCCCCAGCCTTCCACCTCTGCTATTAGGTGCCTGATGTCCTGTACATTTCTCTTTTTCTTTTTCTTTTTTTTTTTTTTTTTTGAGACGGAGTCTTGCTCTGTCGCCCAGATTGGAGTGCAGTGGCACAATCTCGACTCACTGCAAGCTCCGCCTCCCGGGTTCACGCCATTCTTCTGCCTCAGCCACCCGAGTAGCTGGGACTACAGGTGCCCACCACCACACCCGGCTAATTTTTTGTATTTTTTGTAGAGACAGGGTTTTACCGTGTTAGCCAGGATTGTCTCGATCTCCTGACCTTGTGATCTGCCTGCCGTGGCCTCCTAAAGTGCTGGGATTACAGGTGTGAGCCACCACGCCTGGCTAATTTTTTTTTTGTATTTTGAGTAGAGACGGGGTTTCTCCATGTTGGTCAGGCTGGTCTCAAACTCCCAACCTCAGATGATCCACTTGCCTCGGCCTCCTGAAGTGCTGGGATTACAGCTGTACATTTCTTTAGGATTGCAGTTGCTGCACTGTGTCAGGGTGATCTGTTGGCCTGCGATCCCCACCATTAACTGCCTTTACTGTCAGGTACTCATCCATCATTTGTATCCCCGAAGTCCAGCACATGGTAGGTGCTTGGTCAGTGTGTCATGACTGAATGATGAACGTCCATGAGCTACGTAAAGATTAGTGTGAGAGCGAATCTTCCCCAGTAACTTCTTGCAACATTTACTGAGACTAATCACAACTTCCTTATCCCCTCAAAAGATCTCATGGGGTCTTTCTCCTCTTCTCTGATTTAAGCAATGCTACCTTTAGAAATCTGTGGCTATGGCCGGGTGCAGTGGCTCAAGCGTGTAATCCCAGCACTTTAGGAGGCCAAGGCGGGCAGATCACCTGAGGTCGGGAGCTCGAGACCAGCCTGAACAACACAGAGAAACCCCATTTCTATTAAAAATACAAAATTAGCCAGGCGTGGTGGCACATGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCACTTGAACCCGGGAGGCAGAGGTTGCAGTGAGCCGAGATCACATCATTGCACTCCAGCATGGGCAACAAGAGCGAAACTCTGTCTCAAAAAGAAAGAAAGAAATTTGTGGTTACTCTCAGAAGCTGACCCAGCCTGGTTGGGTCAATGACTAGTAGTATCTTCAATTTATGTTACAGATCATGACCAGGCACCGGTGAGCTGGGAGGGGGCTTATGAGGTGGCTGTTGTCTCTGACCCTTGCAG
Seq C2 exon
GTATGAGACAAGACTTTATGAGGATTGGTGCCGGACAGTATCAGAGAAGTCACAGTACAATCTTTCCCAACCACTTCTAAAACGTGACCCAGAGACGAAGGAGATCACTATCAACTTTAACCCACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000007174:ENST00000262442:11
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.083 A=NA C2=0.116
Domain overlap (PFAM):

C1:
PF083857=DHC_N1=FE(4.0=100)
A:
NA
C2:
PF083857=DHC_N1=FE(7.2=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
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

  • Autistic and control brains