Special

HsaEX6047054 @ hg19

Exon Skipping

Gene
Description
dynein, axonemal, heavy chain 8 [Source:HGNC Symbol;Acc:2952]
Coordinates
chr6:38813350-38818190:+
Coord C1 exon
chr6:38813350-38813549
Coord A exon
chr6:38816424-38816577
Coord C2 exon
chr6:38818027-38818190
Length
154 bp
Sequences
Splice sites
3' ss Seq
TTTCCGTTCTTACCTTTTAGATA
3' ss Score
12.35
5' ss Seq
CAGGTAAAT
5' ss Score
8.76
Exon sequences
Seq C1 exon
GATATTTGCATATCTGCCATTAAGGAGAAGGATATCGAAGCCAAGCTGACTCAGGTGATTGAGAATTGGACCAACCAAAATCTGAGTTTTGCAGCATTTAAGGGAAAAGGAGAGCTCCTGCTCAAAGGAACCGAATCGGGAGAAATTATCACTTTGATGGAGGATAGTTTAATGGTCTTAGGGTCTTTACTCAGCAACAG
Seq A exon
ATACAATGCTCCATTTAAAAAAAATATCCAGAATTGGGTGTATAAATTGTCCACTTCCTCAGATATAATTGAAGAGTGGCTCGTAGTACAGAACCTTTGGGTTTATCTTGAAGCCGTCTTTGTAGGTGGAGATATTGCCAAACAGCTGCCTCAG
Seq C2 exon
GAAGCAAAACGTTTTCAGAATATTGACAAGTCTTGGATAAAAATAATGCAGCGAGCTCATGAGAATCCCAATGTGATTAATTGCTGTGTTGGAGATGAAACCATGGGACAACTTTTACCTCATTTACATGAGCAGTTGGAAGTATGTCAGAAGTCACTCACAGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000124721-'37-40,'37-39,38-40=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(16.0=100)
A:
PF083938=DHC_N2=FE(12.3=100)
C2:
PF083938=DHC_N2=FE(13.1=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:
AGGATATCGAAGCCAAGCTGAC
R:
TGGGATTCTCATGAGCTCGCT
Band lengths:
242-396
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains