PAGE5 PAGE family member 5

Information
Symbol
PAGE5
Type
protein-coding
Description
PAGE family member 5
Entrez Gene ID
90737
Genome
hg19
Position
chrX:55,246,788-55,250,539
Genome
hg38
Position
chrX:55,220,355-55,224,106
MIM
301009 OMIM
HGNC
HGNC:29992 HGNC
Ensembl
ENSG00000158639 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
not provided 6 0
Uncertain significance 0 14
Ranking
ClinVar
0
0
0
16
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
SYNONYM CT16.1
SYNONYM CT16.2
SYNONYM GAGEE1
SYNONYM PAGE-5
MIM 301009 OMIM
HGNC HGNC:29992 HGNC
Ensembl ENSG00000158639 Ensembl
AllianceGenome HGNC:29992
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000289619.9 hg38 chrX 55,220,355 55,224,106 3,752
ENST00000374952.1 hg38 chrX 55,220,420 55,224,108 3,689
ENST00000374955.8 hg38 chrX 55,220,346 55,224,108 3,763
ENST00000374955.8 hg19 chrX 55,246,779 55,250,541 3,763
ENST00000289619.9 hg19 chrX 55,246,788 55,250,539 3,752
ENST00000374952.1 hg19 chrX 55,246,853 55,250,541 3,689
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