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 |
---|---|---|---|---|---|
C0027651 | Neoplasms | SDC3 | 9672 | syndecan 3 | O75056 |
C0276496 | Familial Alzheimer Disease (FAD) | SDC3 | 9672 | syndecan 3 | O75056 |
C0235974 | Pancreatic carcinoma | SDC3 | 9672 | syndecan 3 | O75056 |
C1306459 | Primary malignant neoplasm | SDC3 | 9672 | syndecan 3 | O75056 |
C0524620 | Metabolic Syndrome X | SDC3 | 9672 | syndecan 3 | O75056 |
C0003873 | Rheumatoid Arthritis | SDC3 | 9672 | syndecan 3 | O75056 |
C0002395 | Alzheimer's Disease | SDC3 | 9672 | syndecan 3 | O75056 |
C0019196 | Hepatitis C | SDC3 | 9672 | syndecan 3 | O75056 |
C1857276 | Trichohepatoenteric Syndrome | LPIN2 | 9663 | lipin 2 | Q92539 |
C0002876 | Congenital dyserythropoietic anemia | LPIN2 | 9663 | lipin 2 | Q92539 |
C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | LPIN2 | 9663 | lipin 2 | Q92539 |
C0011849 | Diabetes Mellitus | LPIN2 | 9663 | lipin 2 | Q92539 |
C1834531 | MYOPIA 2 (disorder) | LPIN2 | 9663 | lipin 2 | Q92539 |
C0011847 | Diabetes | LPIN2 | 9663 | lipin 2 | Q92539 |
C0002871 | Anemia | LPIN2 | 9663 | lipin 2 | Q92539 |
C0010346 | Crohn Disease | LPIN2 | 9663 | lipin 2 | Q92539 |
C0035021 | Relapsing Fever | LPIN2 | 9663 | lipin 2 | Q92539 |
C0039103 | Synovitis | LPIN2 | 9663 | lipin 2 | Q92539 |
C0028754 | Obesity | LPIN2 | 9663 | lipin 2 | Q92539 |
C0027092 | Myopia | LPIN2 | 9663 | lipin 2 | Q92539 |
C0023530 | Leukopenia | LPIN2 | 9663 | lipin 2 | Q92539 |
C0025517 | Metabolic Diseases | LPIN2 | 9663 | lipin 2 | Q92539 |
C0003873 | Rheumatoid Arthritis | LPIN2 | 9663 | lipin 2 | Q92539 |
C0949116 | Congenital hypoplastic anemia | LPIN2 | 9663 | lipin 2 | Q92539 |
C3714772 | Recurrent fevers | LPIN2 | 9663 | lipin 2 | Q92539 |
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Last updated: August 19, 2024