IPO8 importin 8

Information
Symbol
IPO8
Type
protein-coding
Description
importin 8
Entrez Gene ID
10526
Genome
hg19
Position
chr12:30,781,922-30,848,803
Genome
hg38
Position
chr12:30,628,988-30,695,869
MIM
605600 OMIM
HGNC
HGNC:9853 HGNC
Ensembl
ENSG00000133704 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 34
Likely pathogenic 0 20
Benign 0 8
Likely benign 0 32
Conflicting classifications of pathogenicity 0 2
Uncertain significance 0 86
Ranking
ClinVar
0
0
14
150
8
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM RANBP8
SYNONYM VISS
MIM 605600 OMIM
HGNC HGNC:9853 HGNC
Ensembl ENSG00000133704 Ensembl
AllianceGenome HGNC:9853
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000544829.5 hg38 chr12 30,630,472 30,677,244 46,773
ENST00000256079.9 hg38 chr12 30,628,988 30,695,869 66,882
ENST00000256079.9 hg19 chr12 30,781,922 30,848,803 66,882
ENST00000544829.5 hg19 chr12 30,783,406 30,830,178 46,773
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