Special

HsaEX6063929 @ hg19

Exon Skipping

Gene
Description
potassium channel, subfamily T, member 1 [Source:HGNC Symbol;Acc:18865]
Coordinates
chr9:138676381-138677176:+
Coord C1 exon
chr9:138676381-138676464
Coord A exon
chr9:138676607-138676735
Coord C2 exon
chr9:138677156-138677176
Length
129 bp
Sequences
Splice sites
3' ss Seq
TCAGGGTTCCCACCCTGCAGATG
3' ss Score
7.58
5' ss Seq
GAGGTTCTG
5' ss Score
-0.32
Exon sequences
Seq C1 exon
TCCTTCGTGAAGGACTACATGATCACCATCACCCGGCTGCTGCTGGGCCTGGACACCACGCCGGGCTCGGGGTACCTCTGTGCC
Seq A exon
ATGAAAATCACCGAGGGCGACCTGTGGATCCGCACGTACGGCCGCCTCTTCCAGAAGCTCTGCTCCTCCAGCGCCGAGATCCCCATTGGCATCTACCGGACAGAGAGCCACGTCTTCTCCACCTCGGAG
Seq C2 exon
CCCCACGACCTCAGAGCCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000107147-'30-36,'30-35,31-36=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=0.020 C2=0.143
Domain overlap (PFAM):

C1:
NO
A:
NO
C2:
NO


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
CGTGAAGGACTACATGATCACCA
R:
TGGGCTCTGAGGTCGTGG
Band lengths:
99-228
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains