PAGE3 PAGE family member 3

Information
Symbol
PAGE3
Type
protein-coding
Description
PAGE family member 3
Entrez Gene ID
139793
Genome
hg19
Position
chrX:55,284,848-55,291,349
Genome
hg38
Position
chrX:55,258,415-55,264,916
MIM
300739 OMIM
HGNC
HGNC:4110 HGNC
Ensembl
ENSG00000204279 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
not provided 6 0
Ranking
ClinVar
0
0
0
2
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 CT16.6
SYNONYM GAGED1
SYNONYM PAGE-3
MIM 300739 OMIM
HGNC HGNC:4110 HGNC
Ensembl ENSG00000204279 Ensembl
AllianceGenome HGNC:4110
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000519203.1 hg38 chrX 55,258,478 55,264,730 6,253
ENST00000374951.6 hg38 chrX 55,258,415 55,264,916 6,502
ENST00000374951.6 hg19 chrX 55,284,848 55,291,349 6,502
ENST00000519203.1 hg19 chrX 55,284,911 55,291,163 6,253
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