Special

HsaINT0050093 @ hg38

Intron Retention

Gene
Description
dynein axonemal heavy chain 9 [Source:HGNC Symbol;Acc:HGNC:2953]
Coordinates
chr17:11881209-11883750:+
Coord C1 exon
chr17:11881209-11881413
Coord A exon
chr17:11881414-11883585
Coord C2 exon
chr17:11883586-11883750
Length
2172 bp
Sequences
Splice sites
5' ss Seq
AAGGTGAGG
5' ss Score
9.16
3' ss Seq
CTCTTGCTTGATATTTGCAGTCC
3' ss Score
5.43
Exon sequences
Seq C1 exon
ATTCATTAAAATTGGAGACAAAGAATGTGAATACAATCCCAAGTTCCGGCTCATCCTCCACACCAAGCTGGCTAATCCTCACTACCAGCCTGAGCTGCAGGCTCAGGCCACCCTGATCAACTTCACCGTGACCAGGGATGGCCTGGAGGACCAGTTGCTGGCCGCTGTGGTCAGCATGGAGAGGCCAGACTTGGAGCAGCTGAAG
Seq A exon
GTGAGGACAGAAGGGAGAAAATGTTCTGCCACTAGAGCCTGCAGTGTACTCCACTCTGGGAGAGGTTGCAGAGGGGGGCTGTTTTTCCTGGATTGAGTTAGGTGGGTTCTGCTAGACTCTGGAAGACTGCTGACCCCATGTAGCAACCTGGGAATACCATACTGGGGAAAGAAGGATGGGTGAGCTGAAGAACAGAAGCAAAAACAGTTTGAAGGCCGGGCATGGTGGCTCATGCCTATAATCTGAGCACTTTGGGAGGCCAAGGTGGGCGGATCATGAGGTCGGTAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAAATAAATATTAAAATTAACTGGGCATGGTGGCGCTAGCCTGTAGTCCTAGCTACTCGGGAAGCTGAGGCAGGAGAATCTCTTGAACCCGGGAGACGGAGGTTGCAGTGAGCCAAGATCGTGCCACTGCACTCCAGCCTGGAAATAGGGCGAGGTTCTGTCTCAAAAAAAAGAAAAAAAAAACAGCTTGGAGACTGGACACTCCTATGACCAAGAGCAGAGCCTGGCATGAACATGAGTGCTGCTGATCACACAGGTCCACGTGCCAGAACTAAGCGGAATGAAATTCTACAAGGGTAACAGAACTAGGTCCAACAGTGTTAGGGTCATGTCTTAGCTTGGGCTGCCATAACAAAATACCATAGACGGGGTGGCTTAAATAACACATATTTGTTCTCCTATAATTCTGGAAGTTGGAAGTCTGCGATCATGTTGGTTTTTGGTGAGGCCTCTTTTCCTGCCTTGGAGGCAGCGGCCTTCTCACTGTGACCTCACATGACCTCTTCTTTGCACATAAAGAAAGCCATGGCTCCACCCTGATGACCTCATTTAACCTTAATTACCTCCTTAAAGGCCACATCTCCAATATAGTCACATGGGGGAGTTAAGGCTTCAACATAGGACTTTTAGGACAACACAATTCAATCCACAGCAGATAACGTGCTTTTTGTCCTCTCTTTAAATGTGATTAGATTATACAATATGGCGGGGTCGGTAGGTGGAATTCCAGTGCATGAGAGATTGAGTTCAGGGCTCCCTGGGACTCCGCTTCCTGCAATCATTCATTCATTGAACAGATACCTAGGGAGCACCACCTCTGTAACAGGCAGGATTTGAGGTATGGAGGATTCAGCAGTGAACAAAGAAAACCATGTCCCAGCCTTCATGGAATCTACACTCTAGTGGAGGAACACAGAAAACAGCAACGTAAACAAATGAACAATGCCATTCAGATAGTGATAAGAATTTTTAAGAAAATAAAACAGGGTAATACTGGAAAGCCAGAGGGCAAATTTAAACAGTGGTGGTCAGAAAAAGATTCGGTGAGGAGTTGGCATCTGAGCTAATTCCTAAATAATTGTAAAGCCTCTGGGCATAGAGCATTCCCAGCACAGAGAACAGCAAATCCTGGTCTTAAGGCAGGATCAAGATATGTGGTTTTAAGAAACAAGAAAGGTCAGGGTGGCTGTGGTTGGAACCTCCAACAGGAAGGTTGTTCTTCCCACGAATCCAAAGGCTGTACAAGGGCAAAGACACTACAGCTGCCTGAAGTTAGTGCTTTAGGATATGGAGCATAAAGAGAGGAAGAGATGAGATCCACTTGGATACCAGCACCCCACTCCAGCCTCGAGGAAGCTTTTACACAGTCTGCCATGGTTTTACACAGTTTAAAACTGGAAGACAGATTCTGCTGATTTTTTTTTAAGTAAGCCATAGGAGAGTTGTTCATTAAAGTAAATTGGTAATAGAGAGAACTCTCCAGAGAACTAAAACTGGACCCTAACCCTCTAGTTACACAAATAAGCTCCGTTTAGTGAACACTGATAATGCAGTGTGTTGCCCATTGTGCATTAAGCATAGCACAGAAATCCTAAAAGTTGGGACTGGGATTACAGAAGAGTAAAGAGGGTAAACTGGCTCAAGGTCATGTGCCCAGAATATTGTACAGTTGGGCACCAATTTGACTCCTTGTCTCCTGCTCATGGTCTGAAGCTCTTTGCCATTCTGCCTCCACTTTACTATCTTTAAGGCAAGGGACTCTCGCCCTATTCAGACACATCCTTAGAGCAGGATGCCCTGGGCATCTGCACCTGACTGTCTCTTGCTTGATATTTGCAG
Seq C2 exon
TCCGATCTCACAAAGCAGCAGAATGGATTCAAAATTACCCTGAAAACGTTGGAAGACAGTCTTCTCTCTCGCCTCTCCTCCGCCTCTGGGAACTTCCTGGGAGAAACAGTGCTGGTGGAAAACCTAGAGATCACCAAGCAGACTGCTGCCGAAGTTGAGAAAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000007174:ENST00000262442:55
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.014 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF127812=AAA_9=FE(29.8=100)
A:
NA
C2:
PF127812=AAA_9=PD(22.8=94.5)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
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

  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development