Special

HsaINT0084334 @ hg19

Intron Retention

Gene
Description
potassium voltage-gated channel, subfamily H (eag-related), member 4 [Source:HGNC Symbol;Acc:6253]
Coordinates
chr17:40315624-40316186:-
Coord C1 exon
chr17:40316148-40316186
Coord A exon
chr17:40315977-40316147
Coord C2 exon
chr17:40315624-40315976
Length
171 bp
Sequences
Splice sites
5' ss Seq
CAGGTAACA
5' ss Score
8.88
3' ss Seq
GCTGCCCCCTCTGCCCGCAGCCC
3' ss Score
11.27
Exon sequences
Seq C1 exon
GGCCTCAGCCGCTTTTCCCGATCCCCTCGCCTCTCCCAG
Seq A exon
GTAACACCCACTTCCTGGGTGGGGTTGAATTGCCCTGGGGAGAGGGTGAGATGGGTAGCAGCATCCCCCTTTCCATGGATGGGGAGCTGCATCCGCCGGCGAAGGCTCTTACTTAATGAAGGGGTCTGTTGTTCACTGTCCTGCGACATCAGCTGCCCCCTCTGCCCGCAG
Seq C2 exon
CCCCGCTCAGAAAGCCTCGGCTCCTCCTCAGACAAGACGCTGCCATCCATCACAGAGGCCGAGAGTGGCGCGGAGCCTGGGGGTGGTCCCAGGCCCCGACGGCCCCTCCTGCTGCCCAACCTCAGCCCAGCACGGCCTCGGGGCTCCCTGGTCAGCCTTTTGGGCGAGGAGCTGCCCCCATTCTCAGCCCTTGTCTCCTCTCCTTCCTTATCCCCATCCCTGTCCCCTGCCCTGGCTGGCCAGGGCCACAGTGCCTCCCCTCACGGCCCCCCCAGGTGCTCTGCTGCCTGGAAGCCCCCTCAGCTTCTCATTCCCCCACTGGGAACCTTTGGACCTCCGGACCTCAGTCCCCG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000089558-KCNH4:NM_012285:12
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

Alternative protein isoforms

No structure available
Features
Disorder rate (Iupred):
  C1=0.923 A=NA C2=0.864
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CTCAGCCGCTTTTCCCGATC
R:
GAAGGAGAGGAGACAAGGGCT
Band lengths:
242-413
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