2. Gene
  3. B3GNT7 - UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7 Gene

B3GNT7 - UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7 Gene

  • 基因
  • 蛋白
  • 疾病
  • 相关产品
  • 直系同源

中文名称：UDP-GlcNAc:betaGal beta-1,3-N-乙酰氨基葡萄糖转移酶 7

种属: Homo sapiens

同用名: beta3GnT7

基因 ID: 93010 | 基因类型: protein coding

关于 B3GNT7

Cytogenetic location: 2q37.1 Genomic coordinates (GRCh38): 2:231,395,710-231,401,164 (from NCBI)

This gene has 2 transcripts (splice variants), 194 orthologues and 15 paralogues. Biased expression in colon (RPKM 27.4), stomach (RPKM 7.8) and 8 other tissues.

功能概要

预测启用 UDP-糖基转移酶活性。预计参与聚-N-乙酰基乳糖胺的生物合成过程。预计是膜的组成部分。预测在高尔基体膜中有活性。 [由基因组资源联盟提供，2022 年 4 月]

Predicted to enable UDP-glycosyltransferase activity. Predicted to be involved in poly-N-acetyllactosamine biosynthetic process. Predicted to be integral component of membrane. Predicted to be active in Golgi membrane. [provided by Alliance of Genome Resources, Apr 2022]

B3GNT7 基因产物(1)

mRNA Protein Name
NM_145236.3 NP_660279.1 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7

B3GNT7 蛋白结构

Galactosyl_T

Galactosyl_T: Galactosyltransferase (148 - 343)

  • 0
  • 100
  • 200
  • 300
  • 401 a.a.
蛋白主名 其他名称

UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7

BGnT-7

关联疾病

疾病名称 别名
Macular Dystrophy, Corneal

Macular Corneal Dystrophy

MCD

Corneal Dystrophy, Macular Type

Groenouw Type Ii Corneal Dystrophy

Fehr Corneal Dystrophy

Macular Dystrophy, Corneal Type 1

Mcdc1

Macular Corneal Dystrophy Type Ii

Macular Corneal Dystrophy, Type Ii

Macular Corneal Dystrophy, Type I

Mcdc1, Formerly

Macular Dystrophy, Corneal, 1

Macular Corneal Dystrophy Type 1

Corneal Dystrophy Groenouw Type Ii

Corneal Dystrophy Macular Type

Macular Corneal Dystrophy Type I

Dystrophy, Macular, Corneal
Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, With Or Without Atrial Dysfunction And/Or Dilated Cardiomyopathy

Catecholaminergic Polymorphic Ventricular Tachycardia 1

Ventricular Tachycardia, Catecholaminergic Polymorphic, 1

CPVT1

Ventricular Tachycardia, Stress-Induced Polymorphic

Vtsip

Bidirectional Tachycardia

Stress-Induced Polymorphic Ventricular Tachycardia

Cvpt1

Double Tachycardia Induced By Catecholamines

Malignant Paroxysmal Ventricular Tachycardia

Multifocal Ventricular Premature Beats

Paroxysmal Ventricular Fibrillation

Syncopal Paroxysmal Tachycardia

Syncopal Tachyarythmia

Ventricular Tachycardia Catecholaminergic Polymorphic 1

Tachycardia, Ventricular, Catecholaminergic Polymorphic, Type 1

Multifocal Pvcs

Multifocal Premature Ventricular Beats

Paroxysmal Familial Ventricular Fibrillation

Catecholaminergic Polymorphic Ventricular Tachycardia Type 1
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

相关产品

Pre-clinical Phase
生物活性分子 (1)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-RS01314 B3GNT7 Human Pre-designed siRNA Set A Pre-designed Sets / 否

直系同源

种属 基因名 来源 基因 ID
Mus musculus B3GNT7 MGD MGI:2384394
Felis catus B3GNT7 VGNC VGNC:60059
Canis familiaris B3GNT7 VGNC VGNC:38344
Macaca mulatta B3GNT7 VGNC VGNC:82108
Rattus norvegicus B3GNT7 RGD RGD:1310580
Bos taurus B3GNT7 VGNC VGNC:26383
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