PBX4 PBX homeobox 4

Information
Symbol
PBX4
Type
protein-coding
Description
PBX homeobox 4
Entrez Gene ID
80714
Genome
hg19
Position
chr19:19,672,522-19,729,496
Genome
hg38
Position
chr19:19,561,713-19,618,687
MIM
608127 OMIM
HGNC
HGNC:13403 HGNC
Ensembl
ENSG00000105717 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 50
Ranking
ClinVar
0
0
0
52
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 608127 OMIM
HGNC HGNC:13403 HGNC
Ensembl ENSG00000105717 Ensembl
AllianceGenome HGNC:13403
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000251203.14 hg38 chr19 19,561,713 19,618,687 56,975
ENST00000251203.14 hg19 chr19 19,672,522 19,729,496 56,975
Genome browser