HsaEX6021139 @ hg19
Exon Skipping
Gene
ENSG00000007174 | DNAH9
Description
dynein, axonemal, heavy chain 9 [Source:HGNC Symbol;Acc:2953]
Coordinates
chr17:11671770-11684491:+
Coord C1 exon
chr17:11671770-11671943
Coord A exon
chr17:11672439-11672646
Coord C2 exon
chr17:11684326-11684491
Length
208 bp
Sequences
Splice sites
3' ss Seq
TTATTGTGCTCCCATTCCAGGCG
3' ss Score
9.65
5' ss Seq
AGGGTAAGC
5' ss Score
9.04
Exon sequences
Seq C1 exon
CTTGTGGACTACCGGGCAGAGTTCAGCAAATGGTGGCTGACTGAGTTCAAAACAGTCAAGTTTCCTTCCCAAGGAACCATCTTTGACTATTACATCGACCCAGAGACCAAGAAATTCGAGCCTTGGTCCAAGCTCGTCCCCCAGTTCGAATTTGACCCCGAGATGCCCTTGCAG
Seq A exon
GCGTGTTTGGTGCACACGAGTGAGACCATCCGTGTGTGCTACTTCATGGAGCGGTTGATGGCGCGGCAGCGGCCTGTCATGCTGGTGGGCACGGCTGGCACTGGCAAGTCGGTGCTGGTGGGAGCTAAGCTGGCCAGCCTTGACCCCGAGGCATACCTGGTGAAAAACGTGCCATTCAACTACTACACCACGTCAGCAATGCTGCAGG
Seq C2 exon
CTGTCCTGGAGAAGCCTCTGGAAAAGAAGGCTGGCAGAAACTATGGCCCTCCAGGGAACAAGAAACTCATCTATTTCATTGATGACATGAACATGCCTGAGGTGGATGCCTACGGGACGGTGCAGCCCCACACCATCATCCGGCAGCATCTGGACTATGGCCACTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000007174-'36-38,'36-37,37-38=AN
Average complexity
A_S
Mappability confidence:
100%=100=100%
Protein Impact
ORF disruption upon sequence exclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.000 A=0.000 C2=0.054
Domain overlap (PFAM):
C1:
PF127752=AAA_7=PU(3.3=15.5)
A:
PF127752=AAA_7=FE(25.4=100)
C2:
PF127752=AAA_7=FE(20.2=100)
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:
AGCAAATGGTGGCTGACTGAG
R:
ATAGTCCAGATGCTGCCGGAT
Band lengths:
308-516
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
SPECIAL DATASETS
- Autistic and control brains
Other AS DBs:
FasterDB (Includes CLIP-seq data)
AS-ALPS (AS-induced ALteration of Protein Structure, links to PINs)
APPRIS (Selection of principal isoform)
DEU primates (Only for human)