Special

HsaEX6007400 @ hg19

Exon Skipping

Gene
ENSG00000105877 | DNAH11
Description
dynein, axonemal, heavy chain 11 [Source:HGNC Symbol;Acc:2942]
Coordinates
chr7:21757393-21765602:+
Coord C1 exon
chr7:21757393-21757543
Coord A exon
chr7:21760343-21760474
Coord C2 exon
chr7:21765429-21765602
Length
132 bp
Sequences
Splice sites
3' ss Seq
GACTATTTCTTTTTCTTTAGACT
3' ss Score
8.49
5' ss Seq
CAGGTATGT
5' ss Score
9.8
Exon sequences
Seq C1 exon
GTATGTGGCCAGTTGGATAGACAGAAGGCGGCATCAATCAGAAAAGGCCAATTTGACTATTCTTTTTGATAAATATGTCCCTGCATGCTTGGATAAACTGAGAACAAGCTTTAAAACCATCACTTCAATTCCTGAGAGTAGCCTGGTGCAG
Seq A exon
ACTCTATGTGTTCTTTTGGAGTGCTTGCTGACTCCTGAAAATGTACCTTCTGACAGCCCAAAAGAAGTTTATGAAGTCTATTTTGTATTTGCTTGTATCTGGGCTTTTGGAGGCACCCTGCTACAAGATCAG
Seq C2 exon
ATTTCTGATTATCAAGCTGACTTCAGTCGGTGGTGGCAGAAAGAGATGAAAGCAGTGAAATTTCCGTCGCAGGGAACAATCTTTGATTATTATGTGGACCACAAAACTAAGAAATTATTGCCCTGGGCTGACAAAATTGCCCAGTTTACTATGGATCCAGATGTGCCTCTGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000105877-'50-50,'50-49,51-50=AN
Average complexity
A_S
Mappability confidence:
100%=100=100%
Protein Impact

Alternative protein isoforms (Ref)

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

C1:
NO
A:
NO
C2:
PF127752=AAA_7=PU(3.3=15.5)


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:
TGTCCCTGCATGCTTGGATAA
R:
GCAGAGGCACATCTGGATCCA
Band lengths:
248-380
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains