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 |
Disease ID | Disease Name | Gene Symbol | Gene ID | Gene Name ▲ | UniProt ID |
---|---|---|---|---|---|
C0011880 | Diabetic Ketoacidosis | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
C0024117 | Chronic Obstructive Airway Disease | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
C4048328 | cervical cancer | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
C0020456 | Hyperglycemia | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
C0011581 | Depressive disorder | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
C0677886 | Epithelial ovarian cancer | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
C0025312 | Meningomyelocele | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
C0018790 | Cardiac Arrest | UGCG | 7357 | UDP-glucose ceramide glucosyltransferase | Q16739 |
C0006826 | Malignant Neoplasms | UGGT1 | 56886 | UDP-glucose glycoprotein glucosyltransferase 1 | Q9NYU2 |
C0019196 | Hepatitis C | UGGT1 | 56886 | UDP-glucose glycoprotein glucosyltransferase 1 | Q9NYU2 |
C0600139 | Prostate carcinoma | UGGT1 | 56886 | UDP-glucose glycoprotein glucosyltransferase 1 | Q9NYU2 |
C0947622 | Cholecystolithiasis | UGGT1 | 56886 | UDP-glucose glycoprotein glucosyltransferase 1 | Q9NYU2 |
C0221757 | alpha 1-Antitrypsin Deficiency | UGGT1 | 56886 | UDP-glucose glycoprotein glucosyltransferase 1 | Q9NYU2 |
C0036572 | Seizures | UGGT1 | 56886 | UDP-glucose glycoprotein glucosyltransferase 1 | Q9NYU2 |
C0017551 | Gilbert Disease (disorder) | UGGT1 | 56886 | UDP-glucose glycoprotein glucosyltransferase 1 | Q9NYU2 |
C0002895 | Anemia, Sickle Cell | UGGT1 | 56886 | UDP-glucose glycoprotein glucosyltransferase 1 | Q9NYU2 |
C0271979 | Thalassemia Intermedia | UGGT1 | 56886 | UDP-glucose glycoprotein glucosyltransferase 1 | Q9NYU2 |
C0008350 | Cholelithiasis | UGGT1 | 56886 | UDP-glucose glycoprotein glucosyltransferase 1 | Q9NYU2 |
C0023895 | Liver diseases | UGGT1 | 56886 | UDP-glucose glycoprotein glucosyltransferase 1 | Q9NYU2 |
C0857007 | Hyperbilirubinemia, Neonatal | UGGT1 | 56886 | UDP-glucose glycoprotein glucosyltransferase 1 | Q9NYU2 |
C0010324 | Crigler Najjar syndrome, type 1 | UGGT1 | 56886 | UDP-glucose glycoprotein glucosyltransferase 1 | Q9NYU2 |
C0020433 | Hyperbilirubinemia | UGGT1 | 56886 | UDP-glucose glycoprotein glucosyltransferase 1 | Q9NYU2 |
C0027947 | Neutropenia | UGGT1 | 56886 | UDP-glucose glycoprotein glucosyltransferase 1 | Q9NYU2 |
C0023530 | Leukopenia | UGGT1 | 56886 | UDP-glucose glycoprotein glucosyltransferase 1 | Q9NYU2 |
C0011226 | Hepatitis D Infection | UGGT1 | 56886 | UDP-glucose glycoprotein glucosyltransferase 1 | Q9NYU2 |
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Last updated: August 19, 2024