Special

HsaINT0088128 @ hg38

Intron Retention

Gene
Description
kinesin family member 5B [Source:HGNC Symbol;Acc:HGNC:6324]
Coordinates
chr10:32018502-32019959:-
Coord C1 exon
chr10:32019858-32019959
Coord A exon
chr10:32018563-32019857
Coord C2 exon
chr10:32018502-32018562
Length
1295 bp
Sequences
Splice sites
5' ss Seq
TACGTGAGT
5' ss Score
7.77
3' ss Seq
GTTTGTTCTTCTACTGTTAGGGT
3' ss Score
7.36
Exon sequences
Seq C1 exon
CCAAAACCAGAAAATGATGTTAGAGCAGGAACGTCTAAGAGTAGAACATGAGAAGTTGAAAGCCACAGATCAGGAAAAGAGCAGAAAACTACATGAACTTAC
Seq A exon
GTGAGTAATTGTTTTTAATTAAAGTTTAAAAATAAAAGCTAAATTAGAGGATTATAGGCATTACCTTTGGATATAGCCAGTGGATACATATTTTACTTTGTATGGGCTAAAGGATTTTTTCTTAAATCCACTGAGTTGGTTTGATTTATATCTAAATACTTGGAATATATACTTGCATTTGAGTGAAAGCAAGGTCTTATATTTCATTGTGGTTAAGATTAAGGTTTCTCTTTATTAATCTGCTTGCTGTTTCTTTATCTCCATATTACTTCAGGATCCAGCATAAAAATGAACCTAAAACAATATATTAAGTAACTTCGAAGATTTTAAGATCTAACACAAAAACTGAGTTTTTGTTAAATTTTCTCTTGCATAAAAGAGCATTGTGGTGTTTAGCCTTGCCATTTTGAACAGAGGTTTTCATGGTTTACCTTTTCTCATTTTCTCAAAACTCAGTTTTCTAGAATCTTAGCAGGTAGAAAGTGCATGATTATAATTTTTCACATACCTTGAGTTTGTGAGACAATTTGCAAATCAACTGATATTGTTAGGATAGTTAGAACATCAGGACCAGTTCAGAGTGGATTATATGAAGATTCTGCTAACTTGCAGCTGTAATTTTGTTTAGAATACTTGTAATGTAAAATATTTTAGTCTTTGACAGTTTATAATCTATAATTAATCAGTATCATTTTGGATAAATAGCAGTATAATACATGTGGCATATTTTAAAATATAAATTATAGAACTATTCCTTATTCTTTGAATTCTGCCACATTTTATTTCATCTCTTCCATTGCTATATATGGAATGTATAACAATAGACTGTTGTTTAGAAGGCATATGAAAATTTTTTGAAATTGCAAAGCTGCAGTGGCTCACACCCATAATCTCAGCACTTTGGGAGGCCAGGGCAGGAGAATCAGTTGAGCCCAGTGTTTGAGAATCAGCCTAGGCAATATAGTGAGACCCCGTCTCTACAAAAATTTTTTTAGACAGGGCTGATTGTACATGCCTGTAGTCCCAGCTATTTGGGAGACGAGGTGAGGAGGATCACTTGAGCCCAGGAGGTTGAGGTTGCAGTGAGCAGTGTTTGGGACAGAAACTCTGTGTCAAAAAAAAAAAAATTTTTTTTTTGAAAGACAGCACAGGTAAATTGTTTAAAATAGGCATCTTGTATTTATTTAAATTTAAGAATTTATCCTTTCAGACACAAAATATTTTATTCAACTCTCATGCTAAGTACAATATACAGAATAAAATTTGAAAATATATGTTTGTTCTTCTACTGTTAG
Seq C2 exon
GGTTATGCAAGATAGACGAGAACAAGCAAGACAAGACTTGAAGGGTTTGGAAGAGACAGTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000170759:ENST00000302418:20
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.943 A=NA C2=0.905
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:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
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