Special

HsaEX0020214 @ hg19

Exon Skipping

Gene
Description
dynein, axonemal, heavy chain 8 [Source:HGNC Symbol;Acc:2952]
Coordinates
chr6:38830056-38834453:+
Coord C1 exon
chr6:38830056-38830234
Coord A exon
chr6:38831649-38831836
Coord C2 exon
chr6:38834367-38834453
Length
188 bp
Sequences
Splice sites
3' ss Seq
TTAACTGTTTTTCATGCCAGGTC
3' ss Score
9.98
5' ss Seq
ATGGTGAGA
5' ss Score
7.23
Exon sequences
Seq C1 exon
ATGCTATATCACGTTAGCTCAGGCCTTGGGCATGAACATGGGAGGTGCTCCCGCAGGACCTGCTGGCACTGGCAAAACAGAAACCACAAAAGACATGGGAAGGTGTTTGGGAAAATATGTGGTCGTGTTCAATTGCTCAGATCAAATGGATTTCAGAGGCCTAGGAAGGATTTTCAAAG
Seq A exon
GTCTTGCACAGTCGGGTTCCTGGGGCTGTTTTGATGAGTTTAACAGAATTGAATTGCCTGTATTATCAGTGGCAGCACAACAAATTTATATTGTTTTGACAGCAAGAAAAGAAAGAAAGAAACAGTTCATTTTTTCTGATGGTGATTGTGTTGATTTAAATCCAGAATTTGGAATCTTCTTAACGATG
Seq C2 exon
AACCCTGGATATGCTGGGCGCCAGGAACTACCAGAAAACCTAAAAATCCAGTTTAGAACTGTTGCTATGATGGTTCCTGATAGACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000124721-'45-49,'45-47,46-49
Average complexity
S
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.164 A=0.001 C2=0.000
Domain overlap (PFAM):

C1:
PF127742=AAA_6=FE(25.9=100)
A:
PF127742=AAA_6=FE(26.7=100)
C2:
PF127742=AAA_6=FE(12.1=100)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
ATCACGTTAGCTCAGGCCTTG
R:
TCAGGAACCATCATAGCAACAGT
Band lengths:
252-440
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • The Cancer Genome Atlas (TCGA)
  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development