Special

HsaINT0084401 @ hg19

Intron Retention

Gene
Description
potassium voltage-gated channel, subfamily H (eag-related), member 8 [Source:HGNC Symbol;Acc:18864]
Coordinates
chr3:19491598-19492896:+
Coord C1 exon
chr3:19491598-19491797
Coord A exon
chr3:19491798-19492646
Coord C2 exon
chr3:19492647-19492896
Length
849 bp
Sequences
Splice sites
5' ss Seq
GAGGTAATG
5' ss Score
8.73
3' ss Seq
TCCTTCATCTTCTCTGACAGCTT
3' ss Score
9.61
Exon sequences
Seq C1 exon
CCTTGATGCACGCCTTGGTGTTTGGAAACGTGACAGCAATCATACAGAGGATGTACTCCAGATGGTCCCTCTATCACACTAGAACTAAGGATCTGAAAGATTTCATCCGTGTCCATCACTTGCCCCAACAACTCAAGCAGAGGATGCTCGAATATTTTCAAACAACCTGGTCAGTCAACAATGGAATAGATTCAAATGAG
Seq A exon
GTAATGTTCATTTCTCATGTTGTTTTCAGGCAGAAAGCACATATTCTAAGGTAAACGCAAGATGTTCTAATGCAGGTATCAGAAGTGAAAAGCATACCAACTTCTTTATTCCTTTACATTTTTAATTATTCATGAATCCCAATCCATCTTCTTTCACTTGCTTTGGCTTGTGTTTTCACAATGCCAATTTGGATTGACCGAAGTTTTATATTAACTTGCTGCTTATTCGATCAGGTGGATTTATTTTCCTTCTTATTGTCTCTTTTCAAAGGAATCAATTCTTACGATAATTTAACAGTGTAATCTGGGATAATTATATTAATCAAGTTTCTGTTTCCCTTAACATCAATAAAGTTAAAAAATTCCATCAAAGGGGTTATCTTTATACTTCCAGAAACACCCCAGACTGCCACTATAAAAACAGTATTATATAAATCAACGAACCATTTCATCAACCCACCAGCCAAACCTGTAACCAACATTTTAGTAGTGATTAATTGGTTTCTCCTCTCTTCGCATAATCACCAGTGGGTCCAAATTCCATATCTTCTGTCCTGACTAGGACTCTCTGTGAGAAGGAAGTCACAATGAGTTATATGTTTTCCTGCTAGAGGCTTTTTTAATTTGTTCTGTTTCTCCAGACTTCTTATCAGCTGATTATTCAGTAGCACATAATTCACAGTCACTGAAAAATCTCTCCAGGATTATACATACTTAGATTTCCTCTTCTGTATGCTGGATGGCCAAACAGCAGGAGACAGTAGGAAGAGCATCCCTGCTGTCTTGCAAAGTAAATCAGTTAGACTACACTTACCCCAATTTGATTTCCTCCTTCATCTTCTCTGACAG
Seq C2 exon
CTTTTGAAAGACTTTCCAGATGAACTGCGTTCTGACATCACTATGCACTTGAACAAGGAGATCTTACAGTTGTCCCTTTTTGAATGTGCCAGCCGGGGCTGCCTCAGGTCTCTGTCTCTACACATCAAAACCTCTTTCTGTGCTCCGGGGGAGTATCTGCTGCGTCAAGGGGATGCTTTGCAGGCCATCTACTTTGTATGCTCGGGCTCCATGGAAGTTCTTAAAGACAGCATGGTGCTGGCTATTCTTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000183960-KCNH8:NM_144633:9
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:
PF0052026=Ion_trans=PD(4.7=14.9)
A:
NA
C2:
PF0002724=cNMP_binding=PU(45.5=47.6)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GCCTTGGTGTTTGGAAACGTG
R:
CTTGACGCAGCAGATACTCCC
Band lengths:
358-1207
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development