ZNF2 zinc finger protein 2

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: ZNF2
Type: protein-coding
Description: zinc finger protein 2
Entrez Gene ID: 7549
Genome: hg19
Position: chr2:95,831,562-95,847,919
Genome: hg38
Position: chr2:95,165,817-95,182,171
MIM: 194500 OMIM
HGNC: HGNC:12991 HGNC
Ensembl: ENSG00000275111 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Uncertain significance	4	6

Ranking

	ClinVar
	0
	0
	0
	6
	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

Search Word

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	A1-5
SYNONYM	ZNF661
SYNONYM	Zfp661
MIM	194500 OMIM
HGNC	HGNC:12991 HGNC
Ensembl	ENSG00000275111 Ensembl
AllianceGenome	HGNC:12991

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000611463.1	hg38	chr2	95,165,466	95,184,317	18,852
ENST00000611147.1	hg38	chr2	95,165,817	95,182,171	16,355
ENST00000614034.5	hg38	chr2	95,165,809	95,184,317	18,509
ENST00000622059.4	hg38	chr2	95,165,789	95,182,455	16,667
ENST00000617923.4	hg38	chr2	95,165,432	95,184,317	18,886
ENST00000617923.4	hg19	chr2	95,831,177	95,850,065	18,889
ENST00000611463.1	hg19	chr2	95,831,211	95,850,065	18,855
ENST00000622059.4	hg19	chr2	95,831,534	95,848,203	16,670
ENST00000614034.5	hg19	chr2	95,831,554	95,850,065	18,512
ENST00000611147.1	hg19	chr2	95,831,562	95,847,919	16,358

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