MS4A7 membrane spanning 4-domains A7

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: MS4A7
Type: protein-coding
Description: membrane spanning 4-domains A7
Entrez Gene ID: 58475
Genome: hg19
Position: chr11:60,146,005-60,163,421
Genome: hg38
Position: chr11:60,378,532-60,395,948
MIM: 606502 OMIM
HGNC: HGNC:13378 HGNC
Ensembl: ENSG00000166927 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	20	0
Likely benign	0	2
Uncertain significance	0	22

Ranking

	ClinVar
	0
	0
	0
	24
	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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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	4SPAN2
SYNONYM	CD20L4
SYNONYM	CFFM4
SYNONYM	MS4A8
MIM	606502 OMIM
HGNC	HGNC:13378 HGNC
Ensembl	ENSG00000166927 Ensembl
AllianceGenome	HGNC:13378

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000534016.5	hg38	chr11	60,378,501	60,394,522	16,022
ENST00000300184.8	hg38	chr11	60,378,532	60,395,948	17,417
ENST00000530234.2	hg38	chr11	60,378,539	60,395,254	16,716
ENST00000358246.5	hg38	chr11	60,378,485	60,395,951	17,467
ENST00000358246.5	hg19	chr11	60,145,958	60,163,424	17,467
ENST00000534016.5	hg19	chr11	60,145,974	60,161,995	16,022
ENST00000300184.8	hg19	chr11	60,146,005	60,163,421	17,417
ENST00000530234.2	hg19	chr11	60,146,012	60,162,727	16,716

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