RGS2 regulator of G protein signaling 2

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Information
Clinical Significance
Ranking
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Disease area statistics
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Information

Symbol: RGS2
Type: protein-coding
Description: regulator of G protein signaling 2
Entrez Gene ID: 5997
Genome: hg19
Position: chr1:192,778,169-192,781,405
Genome: hg38
Position: chr1:192,809,039-192,812,275
MIM: 600861 OMIM
HGNC: HGNC:9998 HGNC
Ensembl: ENSG00000116741 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Likely pathogenic	0	2
Benign	4	2
Likely benign	0	2
Uncertain significance	0	14

Ranking

	ClinVar
	0
	0
	0
	20
	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
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	G0S8
MIM	600861 OMIM
HGNC	HGNC:9998 HGNC
Ensembl	ENSG00000116741 Ensembl
AllianceGenome	HGNC:9998

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000235382.7	hg38	chr1	192,809,039	192,812,275	3,237
ENST00000235382.7	hg19	chr1	192,778,169	192,781,405	3,237

Key	Value
strand	+
start	192,778,168
Gene Symbol	RGS2
Entrez GeneId	5,997
Chr Band	1q31
end	192,781,406
chr	chr1

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