Special

HsaEX6042652 @ hg19

Exon Skipping

Gene
Description
dynein, axonemal, heavy chain 3 [Source:HGNC Symbol;Acc:2949]
Coordinates
chr16:21086768-21098381:-
Coord C1 exon
chr16:21098170-21098381
Coord A exon
chr16:21092957-21093048
Coord C2 exon
chr16:21086768-21086882
Length
92 bp
Sequences
Splice sites
3' ss Seq
CTTTCCTCTTTTCTTTGCAGATC
3' ss Score
14.01
5' ss Seq
AAAGTAAGG
5' ss Score
6.6
Exon sequences
Seq C1 exon
GACCCCTCTTCTTACTGAATGCTGAGCAAATTGCGGAGGAGATAGGGAATATGTGGAGGACAACGTATAAACTGATCAAGACCTTGTCTGATGTGCCTGCACCCAGGCGCTTAGCAGAGAATGTGAAGATCAAGATCGATAAGTTCAAGCAGTACATTCCCATCCTCAGTATTTCCTGCAACCCAGGAATGAAAGACCGACACTGGCAGCAG
Seq A exon
ATCAGTGAGATTGTTGGCTATGAGATAAAGCCCACCGAAACGACCTGCCTCTCAAATATGCTCGAATTTGGATTCGGCAAATTCGTTGAAAA
Seq C2 exon
ATTGGAGCCCATTGGTGCAGCTGCCAGCAAGGAATACTCTCTGGAGAAAAACTTGGATAGAATGAAGTTGGATTGGGTTAACGTGACGTTCAGCTTCGTGAAATACAGGGACACT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000158486-'23-25,'23-24,24-25=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:
PF083938=DHC_N2=FE(17.1=100)
A:
PF083938=DHC_N2=FE(7.3=100)
C2:
PF083938=DHC_N2=FE(9.3=100)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GACCTTGTCTGATGTGCCTGC
R:
AGTATTCCTTGCTGGCAGCTG
Band lengths:
171-263
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains