HsaEX6021135 @ hg19
Exon Skipping
Gene
ENSG00000007174 | DNAH9
Description
dynein, axonemal, heavy chain 9 [Source:HGNC Symbol;Acc:2953]
Coordinates
chr17:11687617-11701110:+
Coord C1 exon
chr17:11687617-11687856
Coord A exon
chr17:11696820-11696981
Coord C2 exon
chr17:11700914-11701110
Length
162 bp
Sequences
Splice sites
3' ss Seq
TGTGTCTGTTCCCCTTGAAGGGC
3' ss Score
10.17
5' ss Seq
GATGTGAGT
5' ss Score
7.77
Exon sequences
Seq C1 exon
CGTCACTTCAGCGTGTTTGTCCTCTCCTTCCCGGGGGCAGATGCCCTGTCCTCTATCTACAGCATCATCCTCACTCAGCATCTGAAGCTCGGAAACTTCCCGGCGTCCCTGCAGAAATCCATCCCCCCACTGATCGATCTGGCCCTCGCCTTCCACCAGAAAATTGCTACCACCTTCCTACCCACAGGAATCAAATTCCACTACATCTTCAACCTCAGAGATTTTGCCAACATTTTCCAG
Seq A exon
GGCATTCTCTTCTCCTCAGTGGAATGTGTGAAATCCACATGGGATCTTATAAGGCTCTATCTGCATGAATCAAATCGAGTTTATCGGGATAAGATGGTAGAAGAAAAGGACTTTGATCTTTTTGATAAAATCCAGACAGAAGTGCTCAAGAAAACTTTTGAT
Seq C2 exon
GATATTGAAGACCCTGTGGAGCAGACCCAAAGCCCGAACCTGTATTGTCACTTTGCAAATGGTATTGGGGAGCCCAAATACATGCCTGTACAGTCTTGGGAACTTTTGACCCAGACTCTGGTGGAGGCCTTGGAGAACCACAATGAAGTCAACACAGTGATGGACCTAGTTCTCTTTGAGGATGCCATGCGCCATGT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000007174-'40-42,'40-41,41-42=AN
Average complexity
A_C1
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=0.000
Domain overlap (PFAM):
C1:
PF127752=AAA_7=FE(29.0=100)
A:
PF127752=AAA_7=PD(8.1=40.7)
C2:
PF127802=AAA_8=PU(7.1=28.8)

Main Skipping Isoform:
NA
Other Skipping Isoforms:
NA
Associated events
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
CACTCAGCATCTGAAGCTCGG
R:
GGCTCCCCAATACCATTTGCA
Band lengths:
243-405
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)