Special

HsaEX6042650 @ hg38

Exon Skipping

Gene
Description
dynein axonemal heavy chain 3 [Source:HGNC Symbol;Acc:HGNC:2949]
Coordinates
chr16:21086849-21098769:-
Coord C1 exon
chr16:21098616-21098769
Coord A exon
chr16:21097355-21097499
Coord C2 exon
chr16:21086849-21087060
Length
145 bp
Sequences
Splice sites
3' ss Seq
CATCTCCTTTTGCCCTGCAGTTG
3' ss Score
9.76
5' ss Seq
ATGGTATGT
5' ss Score
8.35
Exon sequences
Seq C1 exon
ATGCTCAGAATTTGAGTTGAGACTTGAGGGCTACCACAGAGAACTGGAAAGTTTTAGGAAGCGCGAAGTGATGACTACAGAAGAAATGAAGCACAATGTTGAAAAGCTTAATGAGCTTTCAAAGAACCTAAATCGGGCGTTTGCAGAGTTTGAG
Seq A exon
TTGATCAATAAGGAGGAAGAGCTATTGGAAAAGGAGAAGAGTACTTACCCTCTTCTGCAGGCCATGCTGAAGAACAAAGTACCTTATGAGCAGCTGTGGTCGACAGCCTATGAGTTCAGCATCAAGTCAGAGGAATGGATGAATG
Seq C2 exon
GACCCCTCTTCTTACTGAATGCTGAGCAAATTGCGGAGGAGATAGGGAATATGTGGAGGACAACGTATAAACTGATCAAGACCTTGTCTGATGTGCCTGCACCCAGGCGCTTAGCAGAGAATGTGAAGATCAAGATCGATAAGTTCAAGCAGTACATTCCCATCCTCAGTATTTCCTGCAACCCAGGAATGAAAGACCGACACTGGCAGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000158486-'28-34,'28-31,29-34
Average complexity
C1
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.019 A=0.000 C2=0.000
Domain overlap (PFAM):

C1:
NO
A:
PF083938=DHC_N2=PU(6.8=57.1)
C2:
PF083938=DHC_N2=FE(17.1=100)


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:
TGAGGGCTACCACAGAGAACT
R:
ACATTCTCTGCTAAGCGCCTG
Band lengths:
254-399
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains