PRRX2 paired related homeobox 2

Information
Symbol
PRRX2
Type
protein-coding
Description
paired related homeobox 2
Entrez Gene ID
51450
Genome
hg19
Position
chr9:132,427,926-132,484,953
Genome
hg38
Position
chr9:129,665,647-129,722,674
MIM
604675 OMIM
HGNC
HGNC:21338 HGNC
Ensembl
ENSG00000167157 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 50
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
SYNONYM PMX2
SYNONYM PRX2
MIM 604675 OMIM
HGNC HGNC:21338 HGNC
Ensembl ENSG00000167157 Ensembl
AllianceGenome HGNC:21338
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000372469.6 hg38 chr9 129,665,647 129,722,674 57,028
ENST00000372469.6 hg19 chr9 132,427,926 132,484,953 57,028
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