BTG4 BTG anti-proliferation factor 4

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Clinical Significance
Ranking
Frequency
Disease area statistics
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Information

Symbol: BTG4
Type: protein-coding
Description: BTG anti-proliferation factor 4
Entrez Gene ID: 54766
Genome: hg19
Position: chr11:111,365,540-111,383,111
Genome: hg38
Position: chr11:111,494,815-111,512,386
MIM: 605673 OMIM
HGNC: HGNC:13862 HGNC
Ensembl: ENSG00000137707 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Pathogenic	0	6
Likely pathogenic	0	4
Likely benign	0	2
Uncertain significance	0	24

Ranking

	ClinVar
	0
	0
	0
	30
	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	APRO3
SYNONYM	OOMD8
SYNONYM	OZEMA8
SYNONYM	PC3B
MIM	605673 OMIM
HGNC	HGNC:13862 HGNC
Ensembl	ENSG00000137707 Ensembl
AllianceGenome	HGNC:13862

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000356018.6	hg38	chr11	111,467,526	111,512,354	44,829
ENST00000689553.1	hg38	chr11	111,495,058	111,514,367	19,310
ENST00000525791.5	hg38	chr11	111,496,512	111,512,339	15,828
ENST00000692032.1	hg38	chr11	111,494,815	111,512,386	17,572
ENST00000356018.6	hg19	chr11	111,338,251	111,383,079	44,829
ENST00000692032.1	hg19	chr11	111,365,540	111,383,111	17,572
ENST00000689553.1	hg19	chr11	111,365,783	111,385,092	19,310
ENST00000525791.5	hg19	chr11	111,367,237	111,383,064	15,828

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