MSN moesin

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: MSN
Type: protein-coding
Description: moesin
Entrez Gene ID: 4478
Genome: hg19
Position: chrX:64,887,521-64,961,793
Genome: hg38
Position: chrX:65,667,654-65,741,931
MIM: 309845 OMIM
HGNC: HGNC:7373 HGNC
Ensembl: ENSG00000147065 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Pathogenic	0	6
Likely pathogenic	0	4
Benign	0	60
Likely benign	0	152
Conflicting classifications of pathogenicity	0	6
not provided	6	0
Uncertain significance	0	168

Ranking

	ClinVar
	0
	0
	18
	364
	4

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	HEL70
SYNONYM	IMD50
MIM	309845 OMIM
HGNC	HGNC:7373 HGNC
Ensembl	ENSG00000147065 Ensembl
AllianceGenome	HGNC:7373

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000360270.7	hg38	chrX	65,667,654	65,741,931	74,278
ENST00000697133.1	hg38	chrX	65,667,624	65,741,925	74,302
ENST00000697138.1	hg38	chrX	65,667,735	65,741,925	74,191
ENST00000697137.1	hg38	chrX	65,667,725	65,741,925	74,201
ENST00000697133.1	hg19	chrX	64,887,491	64,961,787	74,297
ENST00000360270.7	hg19	chrX	64,887,521	64,961,793	74,273
ENST00000697137.1	hg19	chrX	64,887,592	64,961,787	74,196
ENST00000697138.1	hg19	chrX	64,887,602	64,961,787	74,186

Key	Value
strand	+
start	64,887,510
Gene Symbol	MSN
Entrez GeneId	4,478
Chr Band	Xq11.2-q12
end	64,961,792
chr	chrX
Name	moesin

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