HPX hemopexin

Information
Symbol
HPX
Type
protein-coding
Description
hemopexin
Entrez Gene ID
3263
Genome
hg19
Position
chr11:6,452,279-6,462,217
Genome
hg38
Position
chr11:6,431,049-6,440,987
MIM
142290 OMIM
HGNC
HGNC:5171 HGNC
Ensembl
ENSG00000110169 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 20
Likely benign 0 8
Uncertain significance 0 54
Ranking
ClinVar
0
0
0
82
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 HX
MIM 142290 OMIM
HGNC HGNC:5171 HGNC
Ensembl ENSG00000110169 Ensembl
AllianceGenome HGNC:5171
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000265983.8 hg38 chr11 6,431,049 6,440,987 9,939
ENST00000265983.8 hg19 chr11 6,452,279 6,462,217 9,939
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