Special

HsaEX6007402 @ hg19

Exon Skipping

Gene
ENSG00000105877 | DNAH11
Description
dynein, axonemal, heavy chain 11 [Source:HGNC Symbol;Acc:2942]
Coordinates
chr7:21750171-21757543:+
Coord C1 exon
chr7:21750171-21750321
Coord A exon
chr7:21751330-21751478
Coord C2 exon
chr7:21757393-21757543
Length
149 bp
Sequences
Splice sites
3' ss Seq
CAGTGTGCTGCTCACTCCAGGTG
3' ss Score
7.46
5' ss Seq
TCCGTGAGT
5' ss Score
8.93
Exon sequences
Seq C1 exon
GATTGTTTACTCTTATTTTATAGGTCTCTTCTCATCCATTCTACGAGAACAAGCAAATCTTAAGCATGATGGACCAAAATGGATAGTCCTGGATGGCGATATTGACCCCATGTGGATTGAATCACTGAATACTGTAATGGATGATAACAAG
Seq A exon
GTGCTGACCCTCGCCAGCAATGAGCGCATTGCACTCACTCCCTTCATGAGGCTTCTGTTTGAGATACATCACTTAAGGAGCGCAACCCCGGCCACTGTTTCCAGAGCTGGTATTCTGTATGTGAACCCACAAGATCTGGGCTGGAATCC
Seq C2 exon
GTATGTGGCCAGTTGGATAGACAGAAGGCGGCATCAATCAGAAAAGGCCAATTTGACTATTCTTTTTGATAAATATGTCCCTGCATGCTTGGATAAACTGAGAACAAGCTTTAAAACCATCACTTCAATTCCTGAGAGTAGCCTGGTGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000105877-'48-48,'48-47,49-48=AN
Average complexity
A_S
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

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

C1:
PF077289=AAA_5=FE(34.2=100)
A:
PF077289=AAA_5=PD(24.0=70.0)
C2:
NO


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GCAAATCTTAAGCATGATGGACCA
R:
GCACCAGGCTACTCTCAGGAA
Band lengths:
248-397
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains