Special

HsaEX0020109 @ hg38

Exon Skipping

Gene
ENSG00000197653 | DNAH10
Description
dynein axonemal heavy chain 10 [Source:HGNC Symbol;Acc:HGNC:2941]
Coordinates
chr12:123870366-123873710:+
Coord C1 exon
chr12:123870366-123870485
Coord A exon
chr12:123871457-123871602
Coord C2 exon
chr12:123873558-123873710
Length
146 bp
Sequences
Splice sites
3' ss Seq
GTTCCTAATGTCTACTTTAGTTC
3' ss Score
6.39
5' ss Seq
AACGTAAGT
5' ss Score
10.74
Exon sequences
Seq C1 exon
GTCAACTTCCAACCTTGTATGACTTTCATTTTGATAACAAACGGAATCAATGGGTCCCATGGAGTAAATTAGTTCCAGAGTATATTCATGCCCCCGAGAGGAAATTCATCAACATCCTGG
Seq A exon
TTCACACAGTGGATACCACTCGGACTACCTGGATATTGGAACAAATGGTTAAAATTAAGCAACCTGTTATTTTTGTTGGTGAATCTGGCACTTCTAAGACAGCCACTACCCAGAATTTCCTCAAAAATCTGAGTGAAGAAACTAAC
Seq C2 exon
ATTGTGTTAATGGTCAACTTCTCCTCCCGCACCACGTCCATGGATATCCAAAGAAATTTAGAAGCAAATGTGGAAAAGCGAACCAAAGATACTTACGGCCCACCCATGGGAAAACGCCTGCTGGTGTTCATGGATGACATGAATATGCCAAGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000197653_CASSETTE6
Average complexity
S
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=0.061 C2=0.176
Domain overlap (PFAM):

C1:
PF127752=AAA_7=PU(4.8=31.7)
A:
PF127752=AAA_7=FE(17.6=100)
C2:
PF127752=AAA_7=FE(18.4=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:
GTCAACTTCCAACCTTGTATGACT
R:
ATGAACACCAGCAGGCGTTTT
Band lengths:
251-397
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development