ING1 inhibitor of growth family member 1

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Information
Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: ING1
Type: protein-coding
Description: inhibitor of growth family member 1
Entrez Gene ID: 3621
Genome: hg19
Position: chr13:111,367,329-111,373,418
Genome: hg38
Position: chr13:110,714,982-110,721,071
MIM: 601566 OMIM
HGNC: HGNC:6062 HGNC
Ensembl: ENSG00000153487 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Pathogenic	0	6
Benign	0	4
Likely benign	0	4
Uncertain significance	0	66

Ranking

	ClinVar
	0
	0
	0
	74
	6

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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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

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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	p24ING1c
SYNONYM	p33
SYNONYM	p33ING1
SYNONYM	p33ING1b
SYNONYM	p47
SYNONYM	p47ING1a
MIM	601566 OMIM
HGNC	HGNC:6062 HGNC
Ensembl	ENSG00000153487 Ensembl
AllianceGenome	HGNC:6062

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000375774.3	hg38	chr13	110,714,982	110,721,071	6,090
ENST00000375775.4	hg38	chr13	110,713,253	110,720,175	6,923
ENST00000333219.9	hg38	chr13	110,713,700	110,723,339	9,640
ENST00000338450.7	hg38	chr13	110,712,736	110,720,175	7,440
ENST00000715208.1	hg38	chr13	110,713,670	110,723,339	9,670
ENST00000338450.7	hg19	chr13	111,365,083	111,372,522	7,440
ENST00000375775.4	hg19	chr13	111,365,600	111,372,522	6,923
ENST00000715208.1	hg19	chr13	111,366,017	111,375,686	9,670
ENST00000333219.9	hg19	chr13	111,366,047	111,375,686	9,640
ENST00000375774.3	hg19	chr13	111,367,329	111,373,418	6,090

Key	Value
strand	+
UniProt	TSG
start	111,364,969
Gene Symbol	ING1
Entrez GeneId	3,621
Chr Band	13q34
end	111,373,420
chr	chr13

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