Special

HsaINT0049359 @ hg38

Intron Retention

Gene
ENSG00000105877 | DNAH11
Description
dynein axonemal heavy chain 11 [Source:HGNC Symbol;Acc:HGNC:2942]
Coordinates
chr7:21866470-21868007:+
Coord C1 exon
chr7:21866470-21866663
Coord A exon
chr7:21866664-21867858
Coord C2 exon
chr7:21867859-21868007
Length
1195 bp
Sequences
Splice sites
5' ss Seq
CAGGTGGGG
5' ss Score
6.92
3' ss Seq
TATATTCTTGTTTTTTATAGAAA
3' ss Score
8.48
Exon sequences
Seq C1 exon
GCAATTGCCGTCATGGAAGAATTTCGAGGCATAGACCGAGATGTGGAAGGATCTGCCAAGCAGTGGAGGAAGTGGGTAGAATCCGAGTGTCCAGAAAAAGAAAAATTACCTCAAGAATGGAAGAAGAAAAGTTTAATACAGAAGCTGATTCTTCTGAGAGCAATGCGCCCTGACAGAATGACGTATGCTCTCAG
Seq A exon
GTGGGGTGGTCAGCATTTTTGGAAACATGTATTAGTTAACATAGAGGAAATGTAGTCTGAAGAGTTAGGAGGATCTGGTGGAAGTGTTTACCATCCATTTTGATGGGGAGTGATTCTGCTGAGATTTTGATATTATAATCACTGCTACTGTTAAAATTTGCTAAACACTAAACCATGTGCTAGGCAGACTCAGCACATTCTTCCCAAAAAAGCTTAATTCTGAAATCAGTACTGGAGACAGGGGACTGATGGAAATATTCCTGGAAGAGAAATGGGTGTCAGCAGAGTTCAGAGGCCAGGAACATGCATTCATGCATTATCCAAGTGTAATTTCCATCGTTTTCTTTCAGTGATGGCATTTTGGTTCTGAAGATTTTGCATGTCAAACAAAAATGCATTCCTTTCATGGAGTCACTCATAGTCCCTATAACTTTACAACCAATGCAGTTTCAAAGCAGAAACCCTTGTCTACATCTTGGTTTAAGTGTCCTTTTTCTTTGCCCTCTTGGCTTCTAAATGGTAATGTGCTGCTTAATTCACACAAGTCTCATTCTAATTTGAATTCACCAACCAAAGAGTTCTCAACTTCCTTCCCTATTGTGTTTCTTCAGTAATATTCATGTGCCTCAGGTTTTTTCCTTTGCTTTGTCTAGTTCAGCCAATTTTCCCTTTGCAGAAACCTCTGCTGAACTCTACTTTACAAGTTAATTCTGCTTAGTAGTACTTACTTTCTGCTAAATCTGATGCTGCTGGAAAATAATCCTTGCTTAATTGAGCCTCCCTGTGTTAGAAACACCCCAAAAAGCATTTGTATATTCATGAGAAGCCCAGCAGGCTGGAAAATTGCACTGTGGCAAATCTAATGAACTGTTAATAAGTAATGGGGGAATCTGGCAGGGGATTTGGGGGATACAAAGCCATAGCAGACAGCTGATGGCACTCAGGGGGGTCTCAGTAGCCCCCCAAAATGGAATGTAGGCTTCTGATTTTCAGAGCTTCTAAGGAAGAGAAGGATTTCATTGACACACCTACCGCATACATCTAGCTGGATTCATATTGTTATTCTAACAAGACATCCCATGTAATAAACCTGGTTACTTCTATCGTGTGCCTGTGTGGTTTAAGCTTATCCAAATGGTGACTCTTTTCAAGGTCAAAACCACTGATCATGTTTTTATATTCTTGTTTTTTATAG
Seq C2 exon
AAATTTTGTAGAGGAAAAACTGGGTGCGAAGTATGTGGAGAGGACCAGATTGGACTTAGTTAAAGCATTCGAAGAAAGCAGCCCAGCCACCCCCATATTCTTCATCCTGTCTCCGGGGGTAGATGCCCTTAAAGACCTGGAGATTCTTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000105877:ENST00000409508:71
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:
PF0302810=Dynein_heavy=FE(9.1=100)
A:
NA
C2:
PF0302810=Dynein_heavy=FE(7.1=100)


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:
GCAATTGCCGTCATGGAAGAA
R:
AAGAATCTCCAGGTCTTTAAGGGC
Band lengths:
342-1537
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains
  • Pre-implantation embryo development