HsaEX6021125 @ hg19
Exon Skipping
Gene
ENSG00000007174 | DNAH9
Description
dynein, axonemal, heavy chain 9 [Source:HGNC Symbol;Acc:2953]
Coordinates
chr17:11778266-11784730:+
Coord C1 exon
chr17:11778266-11778501
Coord A exon
chr17:11783395-11783517
Coord C2 exon
chr17:11784526-11784730
Length
123 bp
Sequences
Splice sites
3' ss Seq
ACTCATACTTGTTTCCCTAGCTA
3' ss Score
6.71
5' ss Seq
ACGGTAAGA
5' ss Score
10.65
Exon sequences
Seq C1 exon
ACTCCCATTCCAGTCACCCCAGCCCTGGATCCCCTGAGGATGCTGATGGATGATGCTGACGTGGCTGCCTGGCAGAACGAGGGCCTCCCAGCCGACCGCATGTCCGTGGAGAATGCCACCATTCTCATCAACTGTGAGCGCTGGCCACTCATGGTTGACCCTCAGCTACAAGGCATCAAATGGATCAAGAATAAATATGGTGAAGATCTCCGGGTCACGCAGATTGGTCAGAAAGG
Seq A exon
CTACCTTCAAATCATAGAGCAGGCCCTGGAAGCTGGAGCTGTGGTGCTGATTGAAAATCTAGAGGAGTCCATTGATCCTGTTCTGGGACCCCTGCTTGGGAGAGAAGTCATTAAAAAAGGACG
Seq C2 exon
ATTCATTAAAATTGGAGACAAAGAATGTGAATACAATCCCAAGTTCCGGCTCATCCTCCACACCAAGCTGGCTAATCCTCACTACCAGCCTGAGCTGCAGGCTCAGGCCACCCTGATCAACTTCACCGTGACCAGGGATGGCCTGGAGGACCAGTTGCTGGCCGCTGTGGTCAGCATGGAGAGGCCAGACTTGGAGCAGCTGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000007174-'52-54,'52-53,53-54=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=0.014
Domain overlap (PFAM):
C1:
PF127772=MT=PD(2.9=6.3),PF0102514=GrpE=PD(18.6=20.3),PF097314=Mitofilin=PD(1.2=1.3),PF127812=AAA_9=PU(60.7=82.3)
A:
PF127812=AAA_9=FE(18.0=100)
C2:
PF127812=AAA_9=FE(29.8=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:
TCTCATCAACTGTGAGCGCTG
R:
CGGTGAAGTTGATCAGGGTGG
Band lengths:
242-365
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)