NUCB2 nucleobindin 2

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: NUCB2
Type: protein-coding
Description: nucleobindin 2
Entrez Gene ID: 4925
Genome: hg19
Position: chr11:17,298,286-17,353,758
Genome: hg38
Position: chr11:17,276,739-17,332,211
MIM: 608020 OMIM
HGNC: HGNC:8044 HGNC
Ensembl: ENSG00000070081 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Likely benign	0	2
not provided	0	2
Uncertain significance	0	24

Ranking

	ClinVar
	0
	0
	0
	26
	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

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	HEL-S-109
SYNONYM	NEFA
MIM	608020 OMIM
HGNC	HGNC:8044 HGNC
Ensembl	ENSG00000070081 Ensembl
AllianceGenome	HGNC:8044

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000529010.6	hg38	chr11	17,276,739	17,332,211	55,473
ENST00000323688.10	hg38	chr11	17,276,741	17,331,390	54,650
ENST00000529010.6	hg19	chr11	17,298,286	17,353,758	55,473
ENST00000323688.10	hg19	chr11	17,298,288	17,352,937	54,650

Key	Value
strand	+
start	17,298,285
Gene Symbol	NUCB2
Entrez GeneId	4,925
Chr Band	11p15.1
end	17,353,069
chr	chr11

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