HsaEX6021163 @ hg38
Exon Skipping
Gene
ENSG00000007174 | DNAH9
Description
dynein axonemal heavy chain 9 [Source:HGNC Symbol;Acc:HGNC:2953]
Coordinates
chr17:11647072-11653002:+
Coord C1 exon
chr17:11647072-11647198
Coord A exon
chr17:11651069-11651324
Coord C2 exon
chr17:11652761-11653002
Length
256 bp
Sequences
Splice sites
3' ss Seq
GTGTTGCTTCTTTTCTCCAGCTG
3' ss Score
9.48
5' ss Seq
AAGGTAACA
5' ss Score
8.92
Exon sequences
Seq C1 exon
GTATGAGACAAGACTTTATGAGGATTGGTGCCGGACAGTATCAGAGAAGTCACAGTACAATCTTTCCCAACCACTTCTAAAACGTGACCCAGAGACGAAGGAGATCACTATCAACTTTAACCCACAG
Seq A exon
CTGATTTCAGTGCTGAAAGAAATGAGCTATCTTGAACCCAGAGAGATGAAACACATGCCTGAGACAGCAGCAGCCATGTTCTCCTCCAGGGATTTCTATCGGCAGCTTGTGGCTAATTTAGAGTTGATGGCAAATTGGTACAACAAGGTTATGAAAACTCTGCTGGAGGTGGAATTTCCATTAGTGGAGGAAGAGCTGCAAAATATTGATCTCCGCCTCAGAGCAGCAGAGGAGACTTTGAACTGGAAAACAGAAG
Seq C2 exon
GCATTTGCGATTATGTCACTGAAATCACCAGTAGTATTCATGATCTTGAACAAAGAATTCAGAAAACTAAAGACAATGTGGAAGAGATCCAAAACATCATGAAAACATGGGTGACTCCAATATTTAAGACAAAAGATGGAAAAAGGGAATCCCTTCTTTCTCTGGATGATCGGCATGATCGAATGGAAAAATATTACAATCTCATCAAGGAATCTGGCCTTAAGATCCACGCCCTTGTTCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000007174_MULTIEX2-3/12=2-4
Average complexity
S*
Mappability confidence:
100%=100=100%
Protein Impact
ORF disruption upon sequence exclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.116 A=0.012 C2=0.000
Domain overlap (PFAM):
C1:
PF083857=DHC_N1=FE(7.2=100)
A:
PF083857=DHC_N1=FE(14.6=100)
C2:
PF083857=DHC_N1=PD(1.0=7.4)
Main Skipping Isoform:
NA
Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
TAAAACGTGACCCAGAGACGA
R:
CTGAACAAGGGCGTGGATCTT
Band lengths:
292-548
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
SPECIAL DATASETS
- Autistic and control brains