Special

HsaEX0020220 @ hg19

Exon Skipping

Gene
Description
dynein, axonemal, heavy chain 8 [Source:HGNC Symbol;Acc:2952]
Coordinates
chr6:38834367-38835972:+
Coord C1 exon
chr6:38834367-38834453
Coord A exon
chr6:38834545-38834652
Coord C2 exon
chr6:38835838-38835972
Length
108 bp
Sequences
Splice sites
3' ss Seq
CTCACTATATTAATTTTCAGATC
3' ss Score
8.89
5' ss Seq
CAGGTAACT
5' ss Score
8.63
Exon sequences
Seq C1 exon
AACCCTGGATATGCTGGGCGCCAGGAACTACCAGAAAACCTAAAAATCCAGTTTAGAACTGTTGCTATGATGGTTCCTGATAGACAG
Seq A exon
ATCATTATGAGAGTTAAACTTGCAAGCTGTGGTTTTCTTGAAAATGTTATCTTGGCTCAAAAATTTTACGTTCTTTACAAACTCTGTGAAGAGCAACTTACTAAACAG
Seq C2 exon
GTTCATTATGACTTTGGATTGAGAAATATTCTGTCTGTATTGAGGACTCTTGGATCTCAAAAAAGAGCCAGACCAGAAGATAGTGAATTAAGCATTGTCATGAGAGGACTAAGAGATATGAACCTTTCCAAACTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000124721_MULTIEX2-1/2=C1-2
Average complexity
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:
PF127742=AAA_6=FE(12.1=100)
A:
PF127742=AAA_6=FE(15.1=100)
C2:
PF127742=AAA_6=PD(10.3=53.3)


Main Inclusion Isoform:


Main Skipping Isoform:


Other Inclusion Isoforms:


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
AACCCTGGATATGCTGGGCG
R:
TTGGAAAGGTTCATATCTCTTAGTCC
Band lengths:
218-326
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • The Cancer Genome Atlas (TCGA)
  • Autistic and control brains
  • Pre-implantation embryo development