Special

HsaINT0088136 @ hg19

Intron Retention

Gene
Description
kinesin family member 5B [Source:HGNC Symbol;Acc:6324]
Coordinates
chr10:32327091-32327754:-
Coord C1 exon
chr10:32327706-32327754
Coord A exon
chr10:32327147-32327705
Coord C2 exon
chr10:32327091-32327146
Length
559 bp
Sequences
Splice sites
5' ss Seq
ATGGTAAGT
5' ss Score
11.01
3' ss Seq
CATTTGTTTTTCTTTCTCAGTTT
3' ss Score
9.52
Exon sequences
Seq C1 exon
GTTTCATATTTTGAAATATATTTGGATAAGATAAGGGACCTGTTAGATG
Seq A exon
GTAAGTTAAATTCTTGCTAATCAGTTTTAAATAACATCTGTTAATTCCTTTTTAATAATAGATGTGAGACTATTTCTTTGTAACCTATATGAAATTGTCTTAAGTTATTGGAAATAGACAAAATTTTTTTTCTTCTAAAGTTTTAGTTGAATACCTTTAAATAGAATAACTAGTTTAAAGCGATGTTTATGGGTACTTCTTAGTAGTAATTAGAGCATTGGACTGGGAGTTACATAATCTGAGCCCTGAGTTCTAGTCTTCTGTCAACTGTCAATTAGATACATTGTCCTTAGGCAAATCATTGAACCATTCAGGGTTAATGTTCTTGTTTATAAAATGTGGGTGGTAGGTTGGAGTGGTCCTAAAATTCTATATTGTTGCATTGGTTTCTATTTACATCTCCTGCTGTGTCTGTAAGGTCTGCTTTAGAGCAATGTTTTAATATGTTTTTAGAGTTCAACTATTGCTGTTAGGCTGCTCAGGAAAGCCTATCAGTTATTTCATATCCAGTGTTAAGAGTTTTAGGAGAATGTTGCTAACATTTGTTTTTCTTTCTCAG
Seq C2 exon
TTTCAAAGACCAACCTTTCAGTTCATGAAGACAAAAACCGAGTTCCCTATGTAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000170759-KIF5B:NM_004521:5
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:
PF0022518=Kinesin=FE(5.1=100)
A:
NA
C2:
PF0022518=Kinesin=FE(5.8=100)


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