FGF4 fibroblast growth factor 4

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Information

Symbol: FGF4
Type: protein-coding
Description: fibroblast growth factor 4
Entrez Gene ID: 2249
Genome: hg19
Position: chr11:69,585,790-69,590,109
Genome: hg38
Position: chr11:69,771,022-69,775,341
MIM: 164980 OMIM
HGNC: HGNC:3682 HGNC
Ensembl: ENSG00000075388 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	2
Likely benign	0	4
not provided	2	0
Uncertain significance	0	22

Ranking

	ClinVar
	0
	0
	0
	28
	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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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	FGF-4
SYNONYM	HBGF-4
SYNONYM	HST
SYNONYM	HST-1
SYNONYM	HSTF-1
SYNONYM	HSTF1
SYNONYM	K-FGF
SYNONYM	KFGF
MIM	164980 OMIM
HGNC	HGNC:3682 HGNC
Ensembl	ENSG00000075388 Ensembl
AllianceGenome	HGNC:3682

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000168712.3	hg38	chr11	69,771,022	69,775,341	4,320
ENST00000168712.3	hg19	chr11	69,585,790	69,590,109	4,320

Key	Value
strand	-
UniProt	OG
start	69,587,796
Gene Symbol	FGF4
Entrez GeneId	2,249
Chr Band	11q13.3
end	69,590,170
chr	chr11

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