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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 |
|---|---|---|---|---|---|
| C2931826 | Potassium aggravated myotonia | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0032285 | Pneumonia | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0011847 | Diabetes | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0007222 | Cardiovascular Diseases | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0017638 | Glioma | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0033687 | Proteinuria | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0002395 | Alzheimer's Disease | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0020538 | Hypertensive disease | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0003850 | Arteriosclerosis | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0155626 | Acute myocardial infarction | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0038454 | Cerebrovascular accident | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0036572 | Seizures | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0018802 | Congestive heart failure | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0009324 | Ulcerative Colitis | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0007642 | Cellulitis | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0028738 | Nystagmus | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0019163 | Hepatitis B | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0730285 | Diabetic macular edema | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0030442 | Progressive bulbar palsy | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0002736 | Amyotrophic Lateral Sclerosis | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0025958 | Microcephaly | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0020456 | Hyperglycemia | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0021400 | Influenza | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0027051 | Myocardial Infarction | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
