PBX2 PBX homeobox 2

Information
Symbol
PBX2
Type
protein-coding
Description
PBX homeobox 2
Entrez Gene ID
5089
Genome
hg19
Position
chr6:32,152,510-32,157,979
Genome
hg38
Position
chr6:32,184,733-32,190,202
MIM
176311 OMIM
HGNC
HGNC:8633 HGNC
Ensembl
ENSG00000204304 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
not provided 1 0
Uncertain significance 0 30
Ranking
ClinVar
0
0
0
32
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
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 G17
SYNONYM HOX12
SYNONYM PBX2MHC
MIM 176311 OMIM
HGNC HGNC:8633 HGNC
Ensembl ENSG00000204304 Ensembl
AllianceGenome HGNC:8633
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000375050.6 hg38 chr6 32,184,733 32,190,202 5,470
ENST00000375050.6 hg19 chr6 32,152,510 32,157,979 5,470
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