Special

HsaEX6047051 @ hg38

Exon Skipping

Gene
Description
dynein axonemal heavy chain 8 [Source:HGNC Symbol;Acc:HGNC:2952]
Coordinates
chr6:38851572-38853347:+
Coord C1 exon
chr6:38851572-38851674
Coord A exon
chr6:38852694-38852798
Coord C2 exon
chr6:38853186-38853347
Length
105 bp
Sequences
Splice sites
3' ss Seq
CGTTTTCCTCTGTCTTACAGCCG
3' ss Score
10.55
5' ss Seq
GTTGTAATT
5' ss Score
-1.21
Exon sequences
Seq C1 exon
GTATTTGGAGAAGAAACGATTACTGTTTCCAAGATTCTTCTTTGTATCTGATCCAGTTCTCCTGGAAATTCTTGGACAAGCCAGTGATTCCCACACCATACAG
Seq A exon
CCGCATCTCCCTGCAGTATCTGACAACATCAATGAGGTGACATTTCATGCAAAAGACTATGATCGCATCATGGCCGTCATATCAAGAGAAGGAGAAAAAATTGTT
Seq C2 exon
TTGGATAATTCTGTTATGGCCAAAGGTCCTGTGGAGATTTGGCTACTGGATTTGTTAAAAATGCAGATGTCATCATTACATAATATAATTAGATCCGCTTTCTATCAAATCAGTGATTCAGGATTTCAACTCTTACCATTCCTCAGCCACTTTCCAGCACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000124721-'47-48,'47-47,49-48=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:
PF083938=DHC_N2=FE(8.2=100)
A:
PF083938=DHC_N2=FE(8.2=100)
C2:
PF083938=DHC_N2=PD(9.0=68.5)


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:
TGGAGAAGAAACGATTACTGTTTCCA
R:
GCTGGAAAGTGGCTGAGGAAT
Band lengths:
256-361
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains