IMPA2 inositol monophosphatase 2

Information
Symbol
IMPA2
Type
protein-coding
Description
inositol monophosphatase 2
Entrez Gene ID
3613
Genome
hg19
Position
chr18:11,981,506-12,030,876
Genome
hg38
Position
chr18:11,981,507-12,030,877
MIM
605922 OMIM
HGNC
HGNC:6051 HGNC
Ensembl
ENSG00000141401 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Uncertain significance 0 44
Ranking
ClinVar
0
0
0
50
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
MIM 605922 OMIM
HGNC HGNC:6051 HGNC
Ensembl ENSG00000141401 Ensembl
AllianceGenome HGNC:6051
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000625802.2 hg38 chr18 11,981,428 12,008,360 26,933
ENST00000269159.8 hg38 chr18 11,981,507 12,030,877 49,371
ENST00000589238.5 hg38 chr18 11,981,037 12,030,516 49,480
ENST00000588927.5 hg38 chr18 11,981,670 12,030,458 48,789
ENST00000589238.5 hg19 chr18 11,981,036 12,030,515 49,480
ENST00000625802.2 hg19 chr18 11,981,427 12,008,359 26,933
ENST00000269159.8 hg19 chr18 11,981,506 12,030,876 49,371
ENST00000588927.5 hg19 chr18 11,981,669 12,030,457 48,789
Genome browser