IPO4 importin 4

Information
Symbol
IPO4
Type
protein-coding
Description
importin 4
Entrez Gene ID
79711
Genome
hg19
Position
chr14:24,649,425-24,658,022
Genome
hg38
Position
chr14:24,180,219-24,188,816
HGNC
HGNC:19426 HGNC
Ensembl
ENSG00000196497 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 8
Uncertain significance 0 134
Ranking
ClinVar
0
0
0
148
0
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 Imp4
HGNC HGNC:19426 HGNC
Ensembl ENSG00000196497 Ensembl
AllianceGenome HGNC:19426
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000354464.11 hg38 chr14 24,180,219 24,188,816 8,598
ENST00000625289.1 hg38 chr14 24,187,561 24,188,787 1,227
ENST00000354464.11 hg19 chr14 24,649,425 24,658,022 8,598
ENST00000625289.1 hg19 chr14 24,656,767 24,657,993 1,227
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