DisGeNET

DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.

Source Last Updated
DisGeNET July 29, 2024
Displaying entries 46926 - 46950 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C2239176 Liver carcinoma MGAT3 4248 beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase Q09327
C0027651 Neoplasms MGAT3 4248 beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase Q09327
C0006826 Malignant Neoplasms MGAT3 4248 beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase Q09327
C0021390 Inflammatory Bowel Diseases MGAT3 4248 beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase Q09327
C1306459 Primary malignant neoplasm MGAT3 4248 beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase Q09327
C0002395 Alzheimer's Disease MGAT3 4248 beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase Q09327
C0019163 Hepatitis B MGAT3 4248 beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase Q09327
C4721610 Carcinoma, Ovarian Epithelial MGAT3 4248 beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase Q09327
C0919267 ovarian neoplasm MGAT3 4248 beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase Q09327
C0023903 Liver neoplasms MGAT3 4248 beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase Q09327
C1140680 Malignant neoplasm of ovary MGAT3 4248 beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase Q09327
C1862103 Brachydactyly type C MGAT3 4248 beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase Q09327
C0006142 Malignant neoplasm of breast MGAT3 4248 beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase Q09327
C1266044 Collecting Duct Carcinoma of the Kidney MGAT3 4248 beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase Q09327
C3150412 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C4284790 Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies) Type A, 1 B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C3150415 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C0006142 Malignant neoplasm of breast B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C1836373 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C3809042 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13 B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C2875316 Myotubular (centronuclear) myopathy B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C0546264 Congenital Fiber Type Disproportion B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C0002902 Anencephaly B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C0456909 Blindness B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505
C0265221 Walker-Warburg congenital muscular dystrophy B4GAT1 11041 beta-1,4-glucuronyltransferase 1 O43505

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024