GPS2 G protein pathway suppressor 2

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Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: GPS2
Type: protein-coding
Description: G protein pathway suppressor 2
Entrez Gene ID: 2874
Genome: hg19
Position: chr17:7,215,979-7,218,662
Genome: hg38
Position: chr17:7,312,660-7,315,343
MIM: 601935 OMIM
HGNC: HGNC:4550 HGNC
Ensembl: ENSG00000132522 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	4
not provided	4	0
Uncertain significance	0	18

Ranking

	ClinVar
	0
	0
	0
	22
	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	AMF-1
MIM	601935 OMIM
HGNC	HGNC:4550 HGNC
Ensembl	ENSG00000132522 Ensembl
AllianceGenome	HGNC:4550

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000380728.7	hg38	chr17	7,312,661	7,315,360	2,700
ENST00000389167.9	hg38	chr17	7,312,660	7,315,343	2,684
ENST00000389167.9	hg19	chr17	7,215,979	7,218,662	2,684
ENST00000380728.7	hg19	chr17	7,215,980	7,218,679	2,700

Key	Value
strand	-
start	7,215,977
Gene Symbol	GPS2
Entrez GeneId	2,874
Chr Band	17p13
end	7,218,657
chr	chr17

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