Special

HsaINT0076395 @ hg19

Intron Retention

Gene
Description
hexokinase 3 (white cell) [Source:HGNC Symbol;Acc:4925]
Coordinates
chr5:176308693-176309128:-
Coord C1 exon
chr5:176308945-176309128
Coord A exon
chr5:176308849-176308944
Coord C2 exon
chr5:176308693-176308848
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-HK3:NM_002115:16
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:
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