KLK6 kallikrein related peptidase 6

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Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: KLK6
Type: protein-coding
Description: kallikrein related peptidase 6
Entrez Gene ID: 5653
Genome: hg19
Position: chr19:51,461,887-51,472,228
Genome: hg38
Position: chr19:50,958,631-50,968,972
MIM: 602652 OMIM
HGNC: HGNC:6367 HGNC
Ensembl: ENSG00000167755 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	2
Likely benign	0	2
Uncertain significance	0	16

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

[No Data.]

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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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

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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	Bssp
SYNONYM	Klk7
SYNONYM	PRSS18
SYNONYM	PRSS9
SYNONYM	SP59
SYNONYM	hK6
MIM	602652 OMIM
HGNC	HGNC:6367 HGNC
Ensembl	ENSG00000167755 Ensembl
AllianceGenome	HGNC:6367

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000391808.5	hg38	chr19	50,958,632	50,968,791	10,160
ENST00000310157.7	hg38	chr19	50,958,631	50,969,591	10,961
ENST00000594641.1	hg38	chr19	50,959,149	50,968,196	9,048
ENST00000376851.7	hg38	chr19	50,958,631	50,968,972	10,342
ENST00000376851.7	hg19	chr19	51,461,887	51,472,228	10,342
ENST00000310157.7	hg19	chr19	51,461,887	51,472,847	10,961
ENST00000391808.5	hg19	chr19	51,461,888	51,472,047	10,160
ENST00000594641.1	hg19	chr19	51,462,405	51,471,452	9,048

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