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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 |
| Disease ID | Disease Name | Gene Symbol ▼ | Gene ID | Gene Name | UniProt ID |
|---|---|---|---|---|---|
| C0162316 | Iron deficiency anemia | PLA2G6 | 8398 | phospholipase A2 group VI | O60733 |
| C3665347 | Visual Impairment | PLA2G6 | 8398 | phospholipase A2 group VI | O60733 |
| C0577631 | Carotid Atherosclerosis | PLA2G6 | 8398 | phospholipase A2 group VI | O60733 |
| C2239176 | Liver carcinoma | PLA2G6 | 8398 | phospholipase A2 group VI | O60733 |
| C2750220 | Karak Syndrome | PLA2G6 | 8398 | phospholipase A2 group VI | O60733 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | PLA2G6 | 8398 | phospholipase A2 group VI | O60733 |
| C0086445 | Idiopathic Membranous Glomerulonephritis | PLA2G6 | 8398 | phospholipase A2 group VI | O60733 |
| C0494463 | Alzheimer Disease, Late Onset | PLA2G6 | 8398 | phospholipase A2 group VI | O60733 |
| C0027819 | Neuroblastoma | PLA2G6 | 8398 | phospholipase A2 group VI | O60733 |
| C0007097 | Carcinoma | PLA2G6 | 8398 | phospholipase A2 group VI | O60733 |
| C0014070 | Encephalomyelitis | PLA2G6 | 8398 | phospholipase A2 group VI | O60733 |
| C0034152 | Henoch-Schoenlein Purpura | PLA2G6 | 8398 | phospholipase A2 group VI | O60733 |
| C0742343 | Acute Chest Syndrome | PLA2G6 | 8398 | phospholipase A2 group VI | O60733 |
| C0018523 | Hallervorden-Spatz Syndrome | PLA2G6 | 8398 | phospholipase A2 group VI | O60733 |
| C0003850 | Arteriosclerosis | PLA2G6 | 8398 | phospholipase A2 group VI | O60733 |
| C0011849 | Diabetes Mellitus | PLA2G6 | 8398 | phospholipase A2 group VI | O60733 |
| C1853578 | Neuroferritinopathy | PLA2G6 | 8398 | phospholipase A2 group VI | O60733 |
| C2931356 | Spastic paraplegia type 5A, recessive | PLA2G6 | 8398 | phospholipase A2 group VI | O60733 |
| C0017160 | Gastroenteritis | PLA2G6 | 8398 | phospholipase A2 group VI | O60733 |
| C0011581 | Depressive disorder | PLA2G6 | 8398 | phospholipase A2 group VI | O60733 |
| C0037773 | Spastic Paraplegia, Hereditary | PLA2G6 | 8398 | phospholipase A2 group VI | O60733 |
| C0029124 | Optic Atrophy | PLA2G6 | 8398 | phospholipase A2 group VI | O60733 |
| C0004943 | Behcet Syndrome | PLA2G6 | 8398 | phospholipase A2 group VI | O60733 |
| C0011334 | Dental caries | PLA2G6 | 8398 | phospholipase A2 group VI | O60733 |
| C0235946 | Cerebral atrophy | PLA2G6 | 8398 | phospholipase A2 group VI | O60733 |
