Special

HsaINT0076395 @ hg38

Intron Retention

Gene
Description
hexokinase 3 [Source:HGNC Symbol;Acc:HGNC:4925]
Coordinates
chr5:176881692-176882127:-
Coord C1 exon
chr5:176881944-176882127
Coord A exon
chr5:176881848-176881943
Coord C2 exon
chr5:176881692-176881847
Length
96 bp
Sequences
Splice sites
5' ss Seq
GAGGTGTGG
5' ss Score
4.48
3' ss Seq
GTGCACACATGTTCATGCAGGTT
3' ss Score
6.3
Exon sequences
Seq C1 exon
GAACCGGCACCAATGCCTGCTACATGGAGGAGCTCCGGAATGTGGCGGGCGTGCCTGGGGACTCAGGCCGCATGTGCATCAACATGGAGTGGGGCGCCTTTGGGGACGATGGCTCTCTGGCCATGCTCAGCACCCGCTTTGATGCAAGTGTGGACCAGGCGTCCATCAACCCCGGCAAGCAGAG
Seq A exon
GTGTGGGCTGGGCCCAGGCAGTGGTGGCTGGCTGTGACCGGTGCTGGGGATGGTGGCTGGTGGGGCCTTCTGCCGAGTGCACACATGTTCATGCAG
Seq C2 exon
GTTTGAAAAGATGATCAGCGGCATGTACCTGGGGGAGATCGTCCGCCACATCCTTTTACATTTAACCAGCCTTGGCGTTCTCTTCCGGGGCCAGCAGATCCAGCGCCTTCAGACCAGGGACATCTTCAAGACCAAGTTCCTCTCTGAGATCGAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000160883:ENST00000292432:16
Average complexity
IR
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:
PF0372711=Hexokinase_2=FE(25.4=100)
A:
NA
C2:
PF0372711=Hexokinase_2=FE(21.7=100)


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:
TGTGCATCAACATGGAGTGGG
R:
AAAAGGATGTGGCGGACGATC
Band lengths:
169-265
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