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 |
---|---|---|---|---|---|
C0017636 | Glioblastoma | VNN2 | 8875 | vanin 2 | O95498 |
C0015624 | Fanconi Syndrome | VNN2 | 8875 | vanin 2 | O95498 |
C2931187 | Nephropathic cystinosis | VNN2 | 8875 | vanin 2 | O95498 |
C0033860 | Psoriasis | VNN1 | 8876 | vanin 1 | O95497 |
C0025517 | Metabolic Diseases | VNN1 | 8876 | vanin 1 | O95497 |
C0015624 | Fanconi Syndrome | VNN1 | 8876 | vanin 1 | O95497 |
C1306459 | Primary malignant neoplasm | VNN1 | 8876 | vanin 1 | O95497 |
C0009402 | Colorectal Carcinoma | VNN1 | 8876 | vanin 1 | O95497 |
C0178664 | Glomerulosclerosis (disorder) | VNN1 | 8876 | vanin 1 | O95497 |
C0149939 | Obstructive nephropathy | VNN1 | 8876 | vanin 1 | O95497 |
C0004153 | Atherosclerosis | VNN1 | 8876 | vanin 1 | O95497 |
C0699790 | Colon Carcinoma | VNN1 | 8876 | vanin 1 | O95497 |
C0020538 | Hypertensive disease | VNN1 | 8876 | vanin 1 | O95497 |
C0041956 | Ureteral obstruction | VNN1 | 8876 | vanin 1 | O95497 |
C0079731 | B-Cell Lymphomas | VNN1 | 8876 | vanin 1 | O95497 |
C0004096 | Asthma | VNN1 | 8876 | vanin 1 | O95497 |
C0020295 | Hydronephrosis | VNN1 | 8876 | vanin 1 | O95497 |
C0030246 | Pustulosis of Palms and Soles | VNN1 | 8876 | vanin 1 | O95497 |
C0007222 | Cardiovascular Diseases | VNN1 | 8876 | vanin 1 | O95497 |
C0086196 | Eczema, Infantile | VNN1 | 8876 | vanin 1 | O95497 |
C0009319 | Colitis | VNN1 | 8876 | vanin 1 | O95497 |
C0006826 | Malignant Neoplasms | VNN1 | 8876 | vanin 1 | O95497 |
C0398650 | Immune thrombocytopenic purpura | VNN1 | 8876 | vanin 1 | O95497 |
C2931187 | Nephropathic cystinosis | VNN1 | 8876 | vanin 1 | O95497 |
C0021390 | Inflammatory Bowel Diseases | VNN1 | 8876 | vanin 1 | O95497 |
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Last updated: August 19, 2024