PAGE4 PAGE family member 4

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Clinical Significance
Ranking
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Information

Symbol: PAGE4
Type: protein-coding
Description: PAGE family member 4
Entrez Gene ID: 9506
Genome: hg19
Position: chrX:49,593,906-49,598,867
Genome: hg38
Position: chrX:49,829,303-49,834,264
MIM: 300287 OMIM
HGNC: HGNC:4108 HGNC
Ensembl: ENSG00000101951 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	2
not provided	6	0
Uncertain significance	0	4

Ranking

	ClinVar
	0
	0
	0
	6
	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

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Target data	:	MGeND data only
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Variant name	Gene	AA change	CDS	Japanese frequency	TogoVar	MGeND				Genome	ClinVar			CIViC evidence	DisGeNET entry	COSMIC occurrence	Prediction
Variant name	Gene	AA change	CDS	Japanese frequency	TogoVar	Entry	Origin	Type	Annotation	Genome	Entry	Origin	Annotation	CIViC evidence	DisGeNET entry	COSMIC occurrence	Prediction

Search Word

Target data	:	MGeND data only
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Name	MGeND				Type	Genome	Size	Chromosome	Start	Stop	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry
Name	Entry	Origin	Type	Annotation	Type	Genome	Size	Chromosome	Start	Stop	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry

Search Word

Target data	:	MGeND data only
Category	:
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Filtering	:

Name	MGeND				Type	Genome	Gene symbol	Chromosome	Genomic start	Genomic stop	Strand	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry
Name	Entry	Origin	Type	Annotation	Type	Genome	Gene symbol	Chromosome	Genomic start	Genomic stop	Strand	Ref	Alt	ClinVar	Origin	Entry	CIViC evidence	DisGeNET entry

Type	ID
SYNONYM	CT16.7
SYNONYM	GAGE-9
SYNONYM	GAGEC1
SYNONYM	JM-27
SYNONYM	JM27
SYNONYM	PAGE-1
SYNONYM	PAGE-4
MIM	300287 OMIM
HGNC	HGNC:4108 HGNC
Ensembl	ENSG00000101951 Ensembl
AllianceGenome	HGNC:4108

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000376141.5	hg38	chrX	49,829,260	49,833,973	4,714
ENST00000218068.7	hg38	chrX	49,829,303	49,834,264	4,962
ENST00000715210.1	hg38	chrX	49,793,653	49,833,973	40,321
ENST00000715211.1	hg38	chrX	49,793,859	49,833,973	40,115
ENST00000715210.1	hg19	chrX	49,558,256	49,598,576	40,321
ENST00000715211.1	hg19	chrX	49,558,462	49,598,576	40,115
ENST00000376141.5	hg19	chrX	49,593,863	49,598,576	4,714
ENST00000218068.7	hg19	chrX	49,593,906	49,598,867	4,962

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