1. Gene
  2. FUT8 - fucosyltransferase 8 Gene

FUT8 - fucosyltransferase 8 Gene

中文名称:岩藻糖基转移酶 8

种属: Homo sapiens

同用名: CDGF; CDGF1

基因 ID: 2530 | 基因类型: protein coding

关于 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.

功能概要

该基因编码一种属于岩藻糖基转移酶家族的酶。该基因的产物催化岩藻糖从 GDP-岩藻糖转移到 N-连接型复合糖肽。这种酶不同于其他催化 alpha1-2、alpha1-3 和 alpha1-4 岩藻糖加成的岩藻糖基转移酶。该基因的表达可能有助于癌细胞的恶性及其侵袭和转移能力。可变剪接导致多个转录本变体。[RefSeq 提供,2011 年 5 月]

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 基因产物(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
基因本体论
  • 分子功能
  • 生物过程
分子功能 GO 注释 逻辑证据 参考文献 来源
enables glycoprotein 6-alpha-L-fucosyltransferase activity IDA
IDA: 通过直接分析推断
17172260 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
32296183 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in GDP-L-fucose metabolic process IDA
IDA: 通过直接分析推断
17172260 GOA
involved in protein N-linked glycosylation via asparagine IDA
IDA: 通过直接分析推断
17172260 GOA
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断

FUT8 蛋白结构

SH3_9

SH3_9: Variant SH3 domain (509 - 558)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 575 a.a.
蛋白主名 其他名称

alpha-(1,6)-fucosyltransferase

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

FUT8 蛋白互作信息

分类
蛋白名称 蛋白编号 互作蛋白 互作蛋白种属 互作蛋白编号 实验方法 参考文献
种属内
FUT8 Q9BYC5 ZBTB10 Homo sapiens Q96DT7-3 32296183
种属内
FUT8 Q9BYC5 ZBTB10 Homo sapiens Q96DT7-3 32296183
种属间: 跨种属相互作用 种属内: 同种属相互作用

重组 FUT8 蛋白

目录号 产品名 蛋白编号 纯度
HY-P75181 FUT8 Protein, Human (sf9, His) Q9BYC5-1 (R68-K575) ≥95%

关联疾病

疾病名称 别名
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

疾病名称 别名
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

直系同源

种属 基因名 来源 基因 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