MAGED1 MAGE family member D1

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: MAGED1
Type: protein-coding
Description: MAGE family member D1
Entrez Gene ID: 9500
Genome: hg19
Position: chrX:51,636,735-51,645,450
Genome: hg38
Position: chrX:51,893,639-51,902,354
MIM: 300224 OMIM
HGNC: HGNC:6813 HGNC
Ensembl: ENSG00000179222 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	8
Likely benign	0	10
Conflicting classifications of pathogenicity	0	4
not provided	6	0
Uncertain significance	0	56

Ranking

	ClinVar
	0
	0
	0
	74
	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

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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
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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	DLXIN-1
SYNONYM	NRAGE
MIM	300224 OMIM
HGNC	HGNC:6813 HGNC
Ensembl	ENSG00000179222 Ensembl
AllianceGenome	HGNC:6813

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000326587.12	hg38	chrX	51,893,623	51,902,354	8,732
ENST00000375695.2	hg38	chrX	51,893,639	51,902,354	8,716
ENST00000375772.7	hg38	chrX	51,803,007	51,902,354	99,348
ENST00000375722.5	hg38	chrX	51,893,533	51,902,354	8,822
ENST00000375772.7	hg19	chrX	51,546,103	51,645,450	99,348
ENST00000375722.5	hg19	chrX	51,636,629	51,645,450	8,822
ENST00000326587.12	hg19	chrX	51,636,719	51,645,450	8,732
ENST00000375695.2	hg19	chrX	51,636,735	51,645,450	8,716

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