CCRL2 C-C motif chemokine receptor like 2

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

Symbol: CCRL2
Type: protein-coding
Description: C-C motif chemokine receptor like 2
Entrez Gene ID: 9034
Genome: hg19
Position: chr3:46,449,049-46,451,014
Genome: hg38
Position: chr3:46,407,558-46,409,523
MIM: 608379 OMIM
HGNC: HGNC:1612 HGNC
Ensembl: ENSG00000121797 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	2
Likely benign	0	2
Uncertain significance	0	34

Ranking

	ClinVar
	0
	0
	0
	38
	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	ACKR5
SYNONYM	CKRX
SYNONYM	CRAM
SYNONYM	CRAM-A
SYNONYM	CRAM-B
SYNONYM	HCR
MIM	608379 OMIM
HGNC	HGNC:1612 HGNC
Ensembl	ENSG00000121797 Ensembl
AllianceGenome	HGNC:1612

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000399036.4	hg38	chr3	46,407,259	46,409,523	2,265
ENST00000400882.2	hg38	chr3	46,407,881	46,409,522	1,642
ENST00000400880.3	hg38	chr3	46,407,583	46,409,114	1,532
ENST00000357392.4	hg38	chr3	46,407,558	46,409,523	1,966
ENST00000399036.4	hg19	chr3	46,448,750	46,451,014	2,265
ENST00000357392.4	hg19	chr3	46,449,049	46,451,014	1,966
ENST00000400880.3	hg19	chr3	46,449,074	46,450,605	1,532
ENST00000400882.2	hg19	chr3	46,449,372	46,451,013	1,642

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