CXCR6 C-X-C motif chemokine receptor 6

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
Locus Zoom
Variants
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Information

Symbol: CXCR6
Type: protein-coding
Description: C-X-C motif chemokine receptor 6
Entrez Gene ID: 10663
Genome: hg19
Position: chr3:45,986,511-45,989,315
Genome: hg38
Position: chr3:45,945,019-45,947,823
MIM: 605163 OMIM
HGNC: HGNC:16647 HGNC
Ensembl: ENSG00000172215 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	4
Likely benign	0	2
Uncertain significance	0	16

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

[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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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	BONZO
SYNONYM	CD186
SYNONYM	CDw186
SYNONYM	STRL33
SYNONYM	TYMSTR
MIM	605163 OMIM
HGNC	HGNC:16647 HGNC
Ensembl	ENSG00000172215 Ensembl
AllianceGenome	HGNC:16647

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000458629.1	hg38	chr3	45,945,019	45,947,823	2,805
ENST00000438735.1	hg38	chr3	45,940,933	45,948,337	7,405
ENST00000457814.1	hg38	chr3	45,945,049	45,947,510	2,462
ENST00000304552.5	hg38	chr3	45,943,464	45,948,351	4,888
ENST00000438735.1	hg19	chr3	45,982,425	45,989,829	7,405
ENST00000304552.5	hg19	chr3	45,984,956	45,989,843	4,888
ENST00000458629.1	hg19	chr3	45,986,511	45,989,315	2,805
ENST00000457814.1	hg19	chr3	45,986,541	45,989,002	2,462

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