FUT3 fucosyltransferase 3 (Lewis blood group)

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Information
Clinical Significance
Ranking
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Disease area statistics
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Information

Symbol: FUT3
Type: protein-coding
Description: fucosyltransferase 3 (Lewis blood group)
Entrez Gene ID: 2525
Genome: hg19
Position: chr19:5,842,899-5,851,460
Genome: hg38
Position: chr19:5,842,888-5,851,449
MIM: 111100 OMIM
HGNC: HGNC:4014 HGNC
Ensembl: ENSG00000171124 Ensembl
Links: NCBI Gene Cards OncoKB

Clinical Significance

	MGeND	ClinVar
Benign	0	8
Likely benign	0	12
Uncertain significance	0	64

Ranking

	ClinVar
	0
	0
	2
	82
	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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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	CD174
SYNONYM	FT3B
SYNONYM	FucT-III
SYNONYM	LE
SYNONYM	Les
MIM	111100 OMIM
HGNC	HGNC:4014 HGNC
Ensembl	ENSG00000171124 Ensembl
AllianceGenome	HGNC:4014

Descrption	Source	Links

ID	Genome	Chromosome	Start	End	Length
ENST00000458379.7	hg38	chr19	5,842,890	5,851,449	8,560
ENST00000589620.6	hg38	chr19	5,842,888	5,851,449	8,562
ENST00000589918.5	hg38	chr19	5,842,891	5,851,471	8,581
ENST00000303225.12	hg38	chr19	5,842,888	5,851,449	8,562
ENST00000303225.12	hg19	chr19	5,842,899	5,851,460	8,562
ENST00000589620.6	hg19	chr19	5,842,899	5,851,460	8,562
ENST00000458379.7	hg19	chr19	5,842,901	5,851,460	8,560
ENST00000589918.5	hg19	chr19	5,842,902	5,851,482	8,581

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