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 ▼ |
---|---|---|---|---|---|
C0021828 | Intestinal Atresia | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
C0349566 | Squamous cell carcinoma of tongue | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
C0032285 | Pneumonia | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
C0010054 | Coronary Arteriosclerosis | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
C0007131 | Non-Small Cell Lung Carcinoma | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
C0023860 | Listeriosis | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
C0027051 | Myocardial Infarction | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
C1565489 | Renal Insufficiency | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
C1449563 | Cardiomyopathy, Familial Idiopathic | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
C2239176 | Liver carcinoma | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
C0020428 | Hyperaldosteronism | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
C0271650 | Impaired glucose tolerance | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
C0007222 | Cardiovascular Diseases | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
C3714636 | Pneumonitis | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
C0007785 | Cerebral Infarction | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
C0678222 | Breast Carcinoma | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
C0338508 | Optic Atrophy 1 | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
C0017658 | Glomerulonephritis | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
C0007194 | Hypertrophic Cardiomyopathy | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
C0023283 | Leishmaniasis, Cutaneous | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
C3463824 | MYELODYSPLASTIC SYNDROME | GYS1 | 2997 | glycogen synthase 1 | P13807 |
C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | GYS1 | 2997 | glycogen synthase 1 | P13807 |
C0011854 | Diabetes Mellitus, Insulin-Dependent | GYS1 | 2997 | glycogen synthase 1 | P13807 |
C0878544 | Cardiomyopathies | GYS1 | 2997 | glycogen synthase 1 | P13807 |
C0524620 | Metabolic Syndrome X | GYS1 | 2997 | glycogen synthase 1 | P13807 |
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Last updated: August 19, 2024