RRM2 ribonucleotide reductase regulatory subunit M2

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: RRM2
Type: protein-coding
Description: ribonucleotide reductase regulatory subunit M2
Entrez Gene ID: 6241
Genome: hg19
Position: chr2:10,262,455-10,271,545
Genome: hg38
Position: chr2:10,122,328-10,131,418
MIM: 180390 OMIM
HGNC: HGNC:10452 HGNC
Ensembl: ENSG00000171848 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Pathogenic	2	0
Benign	0	2
Uncertain significance	0	14

Ranking

	ClinVar
	0
	0
	0
	16
	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
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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	C2orf48
SYNONYM	R2
SYNONYM	RR2
SYNONYM	RR2M
MIM	180390 OMIM
HGNC	HGNC:10452 HGNC
Ensembl	ENSG00000171848 Ensembl
AllianceGenome	HGNC:10452

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000304567.10	hg38	chr2	10,122,739	10,131,414	8,676
ENST00000360566.6	hg38	chr2	10,122,328	10,131,418	9,091
ENST00000615152.5	hg38	chr2	10,123,171	10,131,414	8,244
ENST00000641198.1	hg38	chr2	10,120,698	10,131,418	10,721
ENST00000360566.6	hg19	chr2	10,262,455	10,271,545	9,091
ENST00000304567.10	hg19	chr2	10,262,866	10,271,541	8,676
ENST00000641198.1	hg19	chr2	10,260,825	10,271,545	10,721
ENST00000615152.5	hg19	chr2	10,263,298	10,271,541	8,244

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