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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 |
|---|---|---|---|---|---|
| C2239176 | Liver carcinoma | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0004153 | Atherosclerosis | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0278878 | Adult Glioblastoma | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0600139 | Prostate carcinoma | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0017154 | Gastritis, Atrophic | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0018801 | Heart failure | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0027651 | Neoplasms | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0524620 | Metabolic Syndrome X | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0002395 | Alzheimer's Disease | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C1336527 | Carcinoma of urinary bladder, superficial | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0020456 | Hyperglycemia | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0026848 | Myopathy | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0029408 | Degenerative polyarthritis | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0235974 | Pancreatic carcinoma | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0020179 | Huntington Disease | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0022658 | Kidney Diseases | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0037116 | Silicosis | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0264694 | Chronic myocardial ischemia | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0235833 | Congenital diaphragmatic hernia | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0020541 | Portal Hypertension | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0034069 | Pulmonary Fibrosis | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0699885 | Carcinoma of bladder | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0011849 | Diabetes Mellitus | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0085584 | Encephalopathies | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0020538 | Hypertensive disease | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
