1. Gene
  2. FUT8 - fucosyltransferase 8 Gene

FUT8 - fucosyltransferase 8 Gene

Homo sapiens

Also known as CDGF; CDGF1

Gene ID: 2530 | Gene type: protein coding

About FUT8

Cytogenetic location: 14q23.3 Genomic coordinates (GRCh38): 14:65,356,842-65,744,121 (from NCBI)

This gene has 17 transcripts (splice variants), 267 orthologues and is associated with 2 phenotypes. Ubiquitous expression in stomach (RPKM 6.3), brain (RPKM 5.7) and 25 other tissues.

Summary

This gene encodes an Enzyme belonging to the family of fucosyltransferases. The product of this gene catalyzes the transfer of fucose from GDP-fucose to N-linked type complex glycopeptides. This Enzyme is distinct from other fucosyltransferases which catalyze alpha1-2, alpha1-3, and alpha1-4 fucose addition. The expression of this gene may contribute to the malignancy of Cancer cells and to their invasive and metastatic capabilities. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2011]

FUT8 Products(6)

mRNA Protein Name
NM_001371533.1 NP_001358462.1 alpha-(1,6)-fucosyltransferase isoform a
NM_001371534.1 NP_001358463.1 alpha-(1,6)-fucosyltransferase isoform a
NM_001371536.1 NP_001358465.1 alpha-(1,6)-fucosyltransferase isoform c
NM_004480.4 NP_004471.4 alpha-(1,6)-fucosyltransferase isoform b
NM_178155.3 NP_835368.1 alpha-(1,6)-fucosyltransferase isoform a
NM_178156.2 NP_835369.1 alpha-(1,6)-fucosyltransferase isoform a

FUT8 Protein Structure

SH3_9

SH3_9: Variant SH3 domain (509 - 558)

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  • 575 a.a.
Protein Preferred Names Protein Names

alpha-(1,6)-fucosyltransferase

GDP-L-Fuc:N-acetyl-beta-D-glucosaminide alpha1,6-fucosyltransferase

Recombinant FUT8 Proteins

Cat. No. Product Name Accession Purity
HY-P75181 FUT8 Protein, Human (sf9, His) Q9BYC5 (R68-K575) ≥95%

Related Diseases

Diseases Alias
Congenital Disorder Of Glycosylation With Defective Fucosylation 1

CDGF1

Cdgf

Lipodystrophy, Congenital Generalized, Type 2

Congenital Generalized Lipodystrophy Type 2

CGL2

Berardinelli-Seip Congenital Lipodystrophy Type 2

Berardinelli-Seip Syndrome

Brunzell Syndrome Bscl2-Related

Total Lipodystrophy And Acromegaloid Gigantism

Berardinelli-Seip Congenital Lipodystrophy, Type 2

Seip Syndrome

Berardinelli Syndrome

Lipodystrophy, Total, And Acromegaloid Gigantism

Lipoatrophic Diabetes, Congenital

Lipodystrophy, Berardinelli-Seip Congenital, Type 2

Brunzell Syndrome, Bscl2-Related

Congenital Lipoatrophic Diabetes

Congenital Generalized Lipodystrophy 2

Lipoatrophic Diabetes

Lipodystrophy Berardinelli Type

Familial Generalized Lipodystrophy

Lipoatrophic Diabetes Mellitus

Familial Partial Lipodystrophy, Type 2

Congenital Disorder Of Glycosylation, Type In

Congenital Disorder Of Glycosylation

CDG1N

Congenital Disorders Of Glycosylation

Cdg In

Cdgin

Congenital Disorder Of Glycosylation 1n

Carbohydrate-Deficient Glycoprotein Syndrome

Cdg

Rft1-Cdg

Cdg-In

Congenital Disorder Of Glycosylation Type In

Carbohydrate Deficient Glycoprotein Syndrome

Cdg Syndrome

Congenital Disorder Of Glycosylation In

Carbohydrate-Deficient Glycoprotein Syndromes

Cdg Syndrome Type In

Carbohydrate Deficient Glycoprotein Syndrome Type In

Congenital Disorder Of Glycosylation Type 1n

Man5glcnac2-Pp-Dol Flippase Deficiency

Glycosylation, Congenital Disorder Of

Glycosylation, Congenital Disorder Of, Type In

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Canis familiaris FUT8 VGNC VGNC:41015
Bos taurus FUT8 VGNC VGNC:29152
Macaca mulatta FUT8 VGNC VGNC:72829
Rattus norvegicus FUT8 RGD RGD:1303096
Mus musculus FUT8 MGD MGI:1858901
Felis catus FUT8 VGNC VGNC:62394
Others FUT8 NCBI