PAGE1 PAGE family member 1

Information
Symbol
PAGE1
Type
protein-coding
Description
PAGE family member 1
Entrez Gene ID
8712
Genome
hg19
Position
chrX:49,452,050-49,460,587
Genome
hg38
Position
chrX:49,687,447-49,695,984
MIM
300288 OMIM
HGNC
HGNC:4107 HGNC
Ensembl
ENSG00000068985 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
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 AL5
SYNONYM CT16.3
SYNONYM GAGE-9
SYNONYM GAGEB1
SYNONYM PAGE-1
MIM 300288 OMIM
HGNC HGNC:4107 HGNC
Ensembl ENSG00000068985 Ensembl
AllianceGenome HGNC:4107
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000376150.4 hg38 chrX 49,687,447 49,695,984 8,538
ENST00000376150.4 hg19 chrX 49,452,050 49,460,587 8,538
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