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 |
---|---|---|---|---|---|
C0032460 | Polycystic Ovary Syndrome | AGPAT2 | 10555 | 1-acylglycerol-3-phosphate O-acyltransferase 2 | O15120 |
C0011854 | Diabetes Mellitus, Insulin-Dependent | AGPAT1 | 10554 | 1-acylglycerol-3-phosphate O-acyltransferase 1 | Q99943 |
C1306459 | Primary malignant neoplasm | AGPAT1 | 10554 | 1-acylglycerol-3-phosphate O-acyltransferase 1 | Q99943 |
C0003873 | Rheumatoid Arthritis | AGPAT1 | 10554 | 1-acylglycerol-3-phosphate O-acyltransferase 1 | Q99943 |
C0023787 | Lipodystrophy | AGPAT1 | 10554 | 1-acylglycerol-3-phosphate O-acyltransferase 1 | Q99943 |
C0006826 | Malignant Neoplasms | AGPAT1 | 10554 | 1-acylglycerol-3-phosphate O-acyltransferase 1 | Q99943 |
C0235974 | Pancreatic carcinoma | AGPAT1 | 10554 | 1-acylglycerol-3-phosphate O-acyltransferase 1 | Q99943 |
C0015695 | Fatty Liver | AGPAT1 | 10554 | 1-acylglycerol-3-phosphate O-acyltransferase 1 | Q99943 |
C0011311 | Dengue Fever | AGPAT1 | 10554 | 1-acylglycerol-3-phosphate O-acyltransferase 1 | Q99943 |
C0026848 | Myopathy | AGL | 178 | amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase | P35573 |
C0017922 | Glycogen Storage Disease Type III | AGL | 178 | amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase | P35573 |
C0878544 | Cardiomyopathies | AGL | 178 | amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase | P35573 |
C0017919 | Glycogen Storage Disease | AGL | 178 | amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase | P35573 |
C0699885 | Carcinoma of bladder | AGL | 178 | amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase | P35573 |
C1968740 | Glycogen Storage Disease IIIB | AGL | 178 | amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase | P35573 |
C1968739 | Glycogen Storage Disease IIIA | AGL | 178 | amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase | P35573 |
C0020615 | Hypoglycemia | AGL | 178 | amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase | P35573 |
C0026850 | Muscular Dystrophy | AGL | 178 | amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase | P35573 |
C0017536 | Giardiasis | AGL | 178 | amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase | P35573 |
C0027651 | Neoplasms | AGL | 178 | amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase | P35573 |
C0041948 | Uremia | AGL | 178 | amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase | P35573 |
C0005695 | Bladder Neoplasm | AGL | 178 | amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase | P35573 |
C1968741 | Glycogen Storage Disease IIIC | AGL | 178 | amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase | P35573 |
C0220989 | Acquired partial lipodystrophy | AGL | 178 | amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase | P35573 |
C0007102 | Malignant tumor of colon | AGL | 178 | amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase | P35573 |
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Last updated: August 19, 2024