HsaEX6071630 @ hg38
Exon Skipping
Gene
ENSG00000140015 | KCNH5
Description
potassium voltage-gated channel subfamily H member 5 [Source:HGNC Symbol;Acc:HGNC:6254]
Coordinates
chr14:63006366-63045455:-
Coord C1 exon
chr14:63045114-63045455
Coord A exon
chr14:63016831-63016954
Coord C2 exon
chr14:63006366-63006472
Length
124 bp
Sequences
Splice sites
3' ss Seq
TTTTCTCCTTTCTTCTTCAGAAT
3' ss Score
12.01
5' ss Seq
CAGGTAGGT
5' ss Score
10.28
Exon sequences
Seq C1 exon
GTTCCCGAGCCCCGTGTGCGGCACCGCCACAGTCTGGGCAGCGGCGGCCGGGGGAGCGCTACTACCATGAACTGCCTGGTCCTCCTCCCCAGAGCTGCTCATCCGGGTCGGGCTGGAGACACAGTCAGGGGACCCCGTCGCCGCCGCCGCGCCCCCTCTTCTTTCGGCTCAATCTTCTCTTCCACCTTTTCCTCCTCTTCCTCCACCTTCTTTGCCTGCATCCCCCCCTCCCCCGCCGCGGATCCTGGCCGCTGCTCTCCAGACCCAGGATGCCGGGGGGCAAGAGAGGGCTGGTGGCACCGCAGAACACATTTTTGGAGAACATCGTCAGGCGCTCCAGTG
Seq A exon
AATCAAGTTTCTTACTGGGAAATGCCCAGATTGTGGATTGGCCTGTAGTTTATAGTAATGACGGTTTTTGTAAACTCTCTGGATATCATCGAGCTGACGTCATGCAGAAAAGCAGCACTTGCAG
Seq C2 exon
TTTTATGTATGGGGAATTGACTGACAAGAAGACCATTGAGAAAGTCAGGCAAACTTTTGACAACTACGAATCAAACTGCTTTGAAGTTCTTCTGTACAAGAAAAACA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000140015-'4-7,'4-5,5-7
Average complexity
C2
Mappability confidence:
100%=100=100%
Protein Impact
ORF disruption upon sequence exclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.080 A=0.000 C2=0.000
Domain overlap (PFAM):
C1:
PF134261=PAS_9=PU(0.9=4.0)
A:
PF134261=PAS_9=FE(37.3=100)
C2:
PF134261=PAS_9=FE(32.7=100)
Main Skipping Isoform:
NA
Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CCCCCTCTTCTTTCGGCTCAA
R:
TGCCTGACTTTCTCAATGGTCT
Band lengths:
242-366
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
SPECIAL DATASETS
- Autistic and control brains