MAPK12 mitogen-activated protein kinase 12

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: MAPK12
Type: protein-coding
Description: mitogen-activated protein kinase 12
Entrez Gene ID: 6300
Genome: hg19
Position: chr22:50,691,330-50,700,112
Genome: hg38
Position: chr22:50,252,901-50,261,683
MIM: 602399 OMIM
HGNC: HGNC:6874 HGNC
Ensembl: ENSG00000188130 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Likely benign	0	4
not provided	1	0
Uncertain significance	0	56

Ranking

	ClinVar
	0
	0
	0
	60
	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
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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	ERK-6
SYNONYM	ERK3
SYNONYM	ERK6
SYNONYM	MAPK 12
SYNONYM	P38GAMMA
SYNONYM	PRKM12
SYNONYM	SAPK-3
SYNONYM	SAPK3
MIM	602399 OMIM
HGNC	HGNC:6874 HGNC
Ensembl	ENSG00000188130 Ensembl
AllianceGenome	HGNC:6874

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000215659.13	hg38	chr22	50,252,901	50,261,683	8,783
ENST00000395780.5	hg38	chr22	50,252,903	50,261,308	8,406
ENST00000395778.3	hg38	chr22	50,257,689	50,261,543	3,855
ENST00000622558.4	hg38	chr22	50,252,903	50,261,716	8,814
ENST00000215659.13	hg19	chr22	50,691,330	50,700,112	8,783
ENST00000395780.5	hg19	chr22	50,691,332	50,699,737	8,406
ENST00000622558.4	hg19	chr22	50,691,332	50,700,145	8,814
ENST00000395778.3	hg19	chr22	50,696,118	50,699,972	3,855

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