PAGE2B PAGE family member 2B

Information
Symbol
PAGE2B
Type
protein-coding
Description
PAGE family member 2B
Entrez Gene ID
389860
Genome
hg19
Position
chrX:55,101,463-55,105,342
Genome
hg38
Position
chrX:55,075,030-55,078,909
HGNC
HGNC:31805 HGNC
Ensembl
ENSG00000238269 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
not provided 6 0
Uncertain significance 0 8
Ranking
ClinVar
0
0
0
10
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 CT16.5
SYNONYM GAGEE3
SYNONYM PAGE-2B
HGNC HGNC:31805 HGNC
Ensembl ENSG00000238269 Ensembl
AllianceGenome HGNC:31805
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000374971.2 hg38 chrX 55,075,030 55,078,909 3,880
ENST00000374974.7 hg38 chrX 55,075,063 55,078,909 3,847
ENST00000374971.2 hg19 chrX 55,101,463 55,105,342 3,880
ENST00000374974.7 hg19 chrX 55,101,496 55,105,342 3,847
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