CCL21 C-C motif chemokine ligand 21

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: CCL21
Type: protein-coding
Description: C-C motif chemokine ligand 21
Entrez Gene ID: 6366
Genome: hg19
Position: chr9:34,709,002-34,710,133
Genome: hg38
Position: chr9:34,709,005-34,710,136
MIM: 602737 OMIM
HGNC: HGNC:10620 HGNC
Ensembl: ENSG00000137077 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	2
Likely benign	0	2
Uncertain significance	0	12

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

[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	6Ckine
SYNONYM	CKb9
SYNONYM	ECL
SYNONYM	SCYA21
SYNONYM	SLC
SYNONYM	TCA4
MIM	602737 OMIM
HGNC	HGNC:10620 HGNC
Ensembl	ENSG00000137077 Ensembl
AllianceGenome	HGNC:10620

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000378792.1	hg38	chr9	34,709,275	34,710,069	795
ENST00000714162.1	hg38	chr9	34,709,005	34,710,136	1,132
ENST00000714163.1	hg38	chr9	34,709,005	34,710,136	1,132
ENST00000259607.7	hg38	chr9	34,709,005	34,710,136	1,132
ENST00000714162.1	hg19	chr9	34,709,002	34,710,133	1,132
ENST00000714163.1	hg19	chr9	34,709,002	34,710,133	1,132
ENST00000259607.7	hg19	chr9	34,709,002	34,710,133	1,132
ENST00000378792.1	hg19	chr9	34,709,272	34,710,066	795

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