Special

HsaINT0084712 @ hg19

Intron Retention

Gene
Description
potassium channel, subfamily T, member 1 [Source:HGNC Symbol;Acc:18865]
Coordinates
chr9:138675870-138676464:+
Coord C1 exon
chr9:138675870-138675971
Coord A exon
chr9:138675972-138676380
Coord C2 exon
chr9:138676381-138676464
Length
409 bp
Sequences
Splice sites
5' ss Seq
CAGGTCAGC
5' ss Score
7.16
3' ss Seq
CTCCCTCCCTCCCTGGCCAGTCC
3' ss Score
9.69
Exon sequences
Seq C1 exon
AGGGAGCGAGAGAATGGCTCCAACCTGGCCTTCATGTTCCGCCTGCCGTTCGCCGCCGGCCGCGTCTTCAGCATCAGCATGTTGGACACACTGCTCTACCAG
Seq A exon
GTCAGCGGGGAAGCGGCAGCAGGAGGGTGGCGCCTGGGTGGGACCCCCGTCATGCCCTCAGCTCTTCAGCCTGGTCCCTGTTCTGAATGATAGGACTCCCTCTGAATGACCTTCCCTGGATTCCAAGGAGACCTCTGGGCCCTGTCCTTGCCCCAGGGATTTCTGGGCCCTTTTTGACCTATGGGTGCCTGGCAAGGGAGTTTTCTTAGAAAAGGCCTCCCAGAACTCTGCCTGTGGGTCATGTGGTGCTTGGGGACCTGGTGGTTCTGTGTGTGTGTATGCATGAGGGGTGGCGAGCCCGTGGCCGGTGGGGTATGGACCTGTGTCCCACGCCCGTGCCCGCGTGCCTCACTGTGGCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCCTGGCCAG
Seq C2 exon
TCCTTCGTGAAGGACTACATGATCACCATCACCCGGCTGCTGCTGGGCCTGGACACCACGCCGGGCTCGGGGTACCTCTGTGCC
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000107147-KCNT1:NM_020822:25
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.000
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
AGCGAGAGAATGGCTCCAACC
R:
GGCACAGAGGTACCCCGAG
Band lengths:
182-591
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains
  • Pre-implantation embryo development