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 44376 - 44400 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0740277 Bile duct carcinoma MGAT5 4249 alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase Q09328
C0278878 Adult Glioblastoma MGAT5 4249 alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase Q09328
C0001430 Adenoma MGAT5 4249 alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase Q09328
C0033687 Proteinuria MGAT5 4249 alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase Q09328
C0279702 Conventional (Clear Cell) Renal Cell Carcinoma MGAT5 4249 alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase Q09328
C0278701 Gastric Adenocarcinoma MGAT5 4249 alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase Q09328
C0700095 Central neuroblastoma MGAT5 4249 alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase Q09328
C1527349 Ductal Breast Carcinoma MGAT5 4249 alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase Q09328
C0855095 Small Lymphocytic Lymphoma MGAT5 4249 alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase Q09328
C0376358 Malignant neoplasm of prostate MGAT5 4249 alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase Q09328
C0011854 Diabetes Mellitus, Insulin-Dependent MGAT5 4249 alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase Q09328
C0038356 Stomach Neoplasms MGAT5 4249 alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase Q09328
C0020459 Hyperinsulinism MGAT5 4249 alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase Q09328
C1621958 Glioblastoma Multiforme MGAT5 4249 alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase Q09328
C0699791 Stomach Carcinoma MGAT5 4249 alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase Q09328
C0017636 Glioblastoma MGAT5 4249 alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase Q09328
C2931008 Congenital disorder of glycosylation type 2A MGAT2 4247 alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase Q10469
C0025517 Metabolic Diseases MGAT2 4247 alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase Q10469
C0036572 Seizures MGAT2 4247 alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase Q10469
C0028754 Obesity MGAT2 4247 alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase Q10469
C0282577 Congenital Disorders of Glycosylation MGAT2 4247 alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase Q10469
C0018784 Sensorineural Hearing Loss (disorder) MGAT2 4247 alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase Q10469
C0027651 Neoplasms MGAT2 4247 alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase Q10469
C0016202 Flatfoot MGAT2 4247 alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase Q10469
C0085207 Gestational Diabetes MGAT2 4247 alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase Q10469

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