IPO7 importin 7

Information
Symbol
IPO7
Type
protein-coding
Description
importin 7
Entrez Gene ID
10527
Genome
hg19
Position
chr11:9,406,199-9,469,674
Genome
hg38
Position
chr11:9,384,652-9,448,127
MIM
605586 OMIM
HGNC
HGNC:9852 HGNC
Ensembl
ENSG00000205339 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 72
Ranking
ClinVar
0
0
0
72
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 Imp7
SYNONYM RANBP7
MIM 605586 OMIM
HGNC HGNC:9852 HGNC
Ensembl ENSG00000205339 Ensembl
AllianceGenome HGNC:9852
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000630083.1 hg38 chr11 9,384,764 9,392,308 7,545
ENST00000379719.8 hg38 chr11 9,384,652 9,448,127 63,476
ENST00000379719.8 hg19 chr11 9,406,199 9,469,674 63,476
ENST00000630083.1 hg19 chr11 9,406,311 9,413,855 7,545
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