PANX2 pannexin 2

Information
Symbol
PANX2
Type
protein-coding
Description
pannexin 2
Entrez Gene ID
56666
Genome
hg19
Position
chr22:50,609,160-50,618,724
Genome
hg38
Position
chr22:50,170,731-50,180,295
MIM
608421 OMIM
HGNC
HGNC:8600 HGNC
Ensembl
ENSG00000073150 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 12
not provided 1 0
Uncertain significance 0 88
Ranking
ClinVar
0
0
0
102
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 PX2
SYNONYM hPANX2
MIM 608421 OMIM
HGNC HGNC:8600 HGNC
Ensembl ENSG00000073150 Ensembl
AllianceGenome HGNC:8600
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000395842.3 hg38 chr22 50,170,731 50,180,295 9,565
ENST00000159647.9 hg38 chr22 50,170,731 50,180,292 9,562
ENST00000159647.9 hg19 chr22 50,609,160 50,618,721 9,562
ENST00000395842.3 hg19 chr22 50,609,160 50,618,724 9,565
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