Special

HsaINT1011599 @ hg38

Intron Retention

Gene
Description
dynein axonemal heavy chain 9 [Source:HGNC Symbol;Acc:HGNC:2953]
Coordinates
chr17:11701122-11704442:+
Coord C1 exon
chr17:11701122-11701247
Coord A exon
chr17:11701248-11704202
Coord C2 exon
chr17:11704203-11704442
Length
2955 bp
Sequences
Splice sites
5' ss Seq
CAGGTATTC
5' ss Score
6.49
3' ss Seq
GGCAACTCTTGCTGCCACAGGTG
3' ss Score
6.91
Exon sequences
Seq C1 exon
GTAGAAATATGGCTGAACCATGTCCTTGGTCACATGAAGGCCACTGTGAGGCATGAGATGACAGAAGGTGTAACTGCCTATGAAGAAAAGCCGAGGGAGCAGTGGCTTTTTGACCACCCAGCTCAG
Seq A exon
GTATTCTCCTAATGGGATCCCCATCCTCCATGGTTGGGGCTGTCTTCCTCCGCAGCCTCCCCCAGCCTTCAGCAGCTGGTAGATATCAGGCTGGCTGCATGCTTCACAGCCAGGGAGGCTTGAATCCCAGACCACTGTGAGGGGTCAGCAGGTGGGAGCAGGGGGATTAACAATAATGACCTAAGTCAACCCTGACCTTGGGAAATCAAGGGTGATCTCTTTTTGCCCTCATTGGCTACAGAAGGGAGAAAATGTCAACAGTTCAACTCTTTGAGCCAGCCTACTTTCTATGTGCCAAGCTCTGTGCTGAGCACAGGACACACCAGTAGGGAACAAGACAATGACACCTGTCTTGCTGGAGTTTACAGACTCATGTGGAACTGAACTGCTGACACATATGACTGGTGTTTTGTTGTTGTTGTTTTGTTTTGTTTTTTGTTTGTTTGTTTAAGACGGGGTGTTGCTCTGTCGCCCAGGCTGAAGTGCAGTGCCACGATGTCGGCTCACTGCAACCTCCACCTCCCAAGTTCAAGCCACTCTCCTGCCTCAGCCTCCCAGGTAGCTGTGACTACAGGCATGCGCCACCAGGGCTGGCTAATTTTTTTTGTATTTTTGGTAGAGATGGGGTTTCACCATGCTGGCCAGGCTGGTCTCAAACTCCTGAACTCAAGTGATCCGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGACGTGAGCCTCCGCGCCCGGCCATGACAGGTGTTTTAATAGGGGAGGCTCAGGGTACTCTGGGAGCATACAGATAGTTCATGAGGTCTGGGGACACGCCCCTGAGCATATGATATGAAAGCTGAGATGTGAAGCAGGAGTTAGCAAGTTAAAAATGGGAGCAAAGAGCAACCAAGTAGGAGGAAGAGCCCAGGCTCAGAAGACAGGGTGAGCAGGTGTGTCTGAGCCAGAGTAAGCGGAGGAGGAGCAAAGGCTGCAGGTGGATTCTGGAAGCCAGTTTCTGTAGACCTTGTGAGAGAGTCTGACTTGATTCTGAGATAGAGTGGAATTCCTTATAGGTTTCTCAGAAGCATAATAAGAGAGAAGCCAGACCTAACAAGAAATGTTTAAAGTAACTCTGGCTACAGTAGGCCACTCCTCCTTCCCTCAGTTAACAGTATAGTAGTAGTGTTGCTCTGTTTGGGGGTTGCAGACATTTAGTAGTCATCAAAGCCATAGAGTAGATAAGATTGCCCTTGCAAAGTATGTAGAATGAGAAGAGAGTGCAGAACAAATTCTTGAGCATCATTCAGAGCCAGAGGAGGAGGAAGGAGGAACCAGTAAAGCAGAATAAGAAATGGTCTTTTGGGAGCAGAAGGAAAACCGGGAAACAGTAATCATGGAAACCAAGCAAGAAACTGTTGGTAGCAGGTAAGAGGTAGGAAATGTCAAACACTTCTAAGAGATGAAGCAAAATAAAGAGGATGAAGAAGGTTCATGGATAAACTTGGTGAGGCCATTTCAGGGGAGTGGTAGGGAAGGGGCCACATTGCAGGGGCTGAGGAGTGGGAAAAGGTAGAAAGTATTCACAGTGGCTGGGCGTGATGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGTGGATCACGAGGTCAGGAGATCGAGACCATCCTGCCTAACACGGTGAAACCCCGTCTCTACTAAAAAATACAAAAAATTAGCCAGGCGTGGTGGTGGGCACCTGTAGTCCCAGCTACTCAGGACGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCGGAGCTTGCAGTAAGCTGAGATCGTGCCACTGCACTCCAGCCTGGGTGACAGAGCGAGACTGTCTCAAAAAAAAAAAAAAAAGAAAAGAAAAGAAAGTATTCACAGTGAATGTGTGTGAATAGCAGGGAGAAACTTGGCTACGAAGAAGAGAGGAGAAAGGAGTCCACACTGCAGAGAAGAAGAGGTGTTTATTAATAGTAGGATTGGAACATCCTCTCAAGTTATCCCAGTAAGGCTGCCAATGAGGGGGAGCTTCTTTAATAAAATCTAATGGGACATAAACTCAAAGGGAAAAATGGACAAACAGAAATGGTGCTGTTTACTACGATGAGATTCTCCATTTCACAAAGGGAGTAAATCCCATCAGGCTTCCTTGTTTACCTGTATCAGAATTTTGAGACAAGAGAATGTGTTGCCTCCTCCTATTGCAGTAAATGTCATCTAGAGTGGTGTCCCCCAAACCAAATGATACTACAGATGAGCAATGGATCTAAATTCCCCACCATGAGTAATCAAAGTTATGCATGTTCCATACAAAGCTTTCCAGCAAATAGAAGAAATATGTATTTCAATTGCTTTTTCTATTTATTTATTTTTAATCTCTGAAAATGCAAATCATATTAACCACAATTGAATTTCAATATCTCTCATCTTGGCACTTAAAAATAGGCACTTTAAGGTTTTAAAATATCTTTAAAATGTAGTGAAAGTATGGTAGAAGAGCAAATGTGTGCCACAGATGATCAGCAGTGGCTCACTAAATTAGGTTGTCAGACCACAGAGGAGCAGAAGACTGGGTGTCATTGGGATGGTTGGGCAACATATTGTCATCCTCCCAAGCTTGGGAAAGTTGCTACCTTTGGGAAGTAAAAGACTGATTCATCCCCGTCACAATTTCTAGAAGGCACCGGCCTTGATCAGAGTCAATCTTGGGTTCTTCTCAACCGAATGATACATTTTTTCAGGAGCAGAAAGTGCTTTTCCCACCTGTACCGCAACAACTTCACACCTTCAAGGGTTTAGAGCATATGGTTCACTTAGTCAGTGCTGGTGGAAGAGGGAGGGATGGGGCTCATGTCACCCACACAATTACATCCTGAGCCCTTGCTGTGTGATGAGTGGGTTGGTTGGAAACAGCCATGATAACAGCTTTACTAGGCAACTCTTGCTGCCACAG
Seq C2 exon
GTGGCCCTGACCTGTACTCAGATCTGGTGGACAACAGAAGTGGGCATGGCATTTGCCAGGCTGGAGGAAGGCTATGAGAGTGCCATGAAGGACTATTATAAGAAGCAAGTGGCCCAGCTCAAAACCCTTATCACCATGCTGATTGGCCAGCTCTCCAAGGGAGACCGGCAGAAGATTATGACTATATGCACCATCGATGTGCATGCCCGGGATGTGGTAGCCAAGATGATTGCTCAGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000007174:ENST00000262442:24
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.048 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF083938=DHC_N2=PD(6.5=64.3)
A:
NA
C2:
NO


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