Special

HsaINT0049299 @ hg19

Intron Retention

Gene
ENSG00000105877 | DNAH11
Description
dynein, axonemal, heavy chain 11 [Source:HGNC Symbol;Acc:2942]
Coordinates
chr7:21640628-21641236:+
Coord C1 exon
chr7:21640628-21640797
Coord A exon
chr7:21640798-21641013
Coord C2 exon
chr7:21641014-21641236
Length
216 bp
Sequences
Splice sites
5' ss Seq
CAGGTAGCC
5' ss Score
7.13
3' ss Seq
TGTACATATATATTTAATAGTCT
3' ss Score
4.34
Exon sequences
Seq C1 exon
ATTGACATTTATGAAGCTTTGTATGTTCAAATGAGCAAATTTGAGGACTTTAGAGTGTTTGATAGTTGGTTCAAGGTGGACATGAAGCCTTTCAAAGTGAGCTTGTTAACCATAATTAAGAAATGGAGCTGGATGTTTCAGGAGCATCTTTTGAGATTTGTCATTGACAG
Seq A exon
GTAGCCTTTTACTTTGGTTTTTGGAATTATAACTTTCTAAACTGCTTTCTAAAACTGAGATGTTACTTTTAAGCGTATTAATGTTGCCAGTTTCATGATAGAGATAAATGTTTAATCAGGTACATAATGAAAATAAGATTCAATCAGAAGTCTTATACTGCTAAATGTTTTAATAAACTTAATTTGTGTGTATCTATGTACATATATATTTAATAG
Seq C2 exon
TCTGAATGAGCTACAAGAATTTATAAAGGAGACAGATTCCGGACTTCAGAGAGAATTAAATGAAGGTGATCATGATGGTTTAGTTGACATCATGGTGCATCTTCTGGCTGTAAGAAGCCGACAGAGAGCTACTGATGAACTCTTTGAACCTCTAAAAGAAACGATCACCCTCTTGGAAAGCTATGGCCAGAAGATGCCTGAGCAGGTCTATATTCAGCTAGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000105877-DNAH11:NM_003777:17
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.040
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TGGTTCAAGGTGGACATGAAGC
R:
GGCCATAGCTTTCCAAGAGGG
Band lengths:
292-508
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