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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 |
|---|---|---|---|---|---|
| C0011884 | Diabetic Retinopathy | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0024623 | Malignant neoplasm of stomach | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0007766 | Intracranial Aneurysm | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0035222 | Respiratory Distress Syndrome, Adult | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0546837 | Malignant neoplasm of esophagus | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0001339 | Acute pancreatitis | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0007131 | Non-Small Cell Lung Carcinoma | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C1800706 | Idiopathic Pulmonary Fibrosis | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0155626 | Acute myocardial infarction | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0025500 | Mesothelioma | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C3203102 | Idiopathic pulmonary arterial hypertension | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0011854 | Diabetes Mellitus, Insulin-Dependent | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0028754 | Obesity | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0019061 | Hemolytic-Uremic Syndrome | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C1145628 | Autonomic nervous system disorders | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0013264 | Muscular Dystrophy, Duchenne | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C3714636 | Pneumonitis | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0023895 | Liver diseases | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0239946 | Fibrosis, Liver | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0038454 | Cerebrovascular accident | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0009319 | Colitis | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0948008 | Ischemic stroke | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0007097 | Carcinoma | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0010054 | Coronary Arteriosclerosis | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0034067 | Pulmonary Emphysema | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
