PAGE2 PAGE family member 2

Information
Symbol
PAGE2
Type
protein-coding
Description
PAGE family member 2
Entrez Gene ID
203569
Genome
hg19
Position
chrX:55,115,451-55,119,275
Genome
hg38
Position
chrX:55,089,018-55,092,842
MIM
300738 OMIM
HGNC
HGNC:31804 HGNC
Ensembl
ENSG00000234068 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
not provided 6 0
Uncertain significance 0 12
Ranking
ClinVar
0
0
0
18
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 CT16.4
SYNONYM GAGEC2
SYNONYM GAGEE2
SYNONYM PAGE-2
MIM 300738 OMIM
HGNC HGNC:31804 HGNC
Ensembl ENSG00000234068 Ensembl
AllianceGenome HGNC:31804
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000374965.5 hg38 chrX 55,089,052 55,092,842 3,791
ENST00000374968.9 hg38 chrX 55,089,018 55,092,842 3,825
ENST00000374968.9 hg19 chrX 55,115,451 55,119,275 3,825
ENST00000374965.5 hg19 chrX 55,115,485 55,119,275 3,791
Genome browser