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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 |
|---|---|---|---|---|---|
| C0034067 | Pulmonary Emphysema | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0035078 | Kidney Failure | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0279671 | Cervical Squamous Cell Carcinoma | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0006826 | Malignant Neoplasms | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0151744 | Myocardial Ischemia | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C1510586 | Autism Spectrum Disorders | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0302592 | Cervix carcinoma | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0008479 | Chondrosarcoma | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0003864 | Arthritis | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0812413 | Malignant Pleural Mesothelioma | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0162871 | Aortic Aneurysm, Abdominal | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C1861172 | Venous Thromboembolism | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0014522 | Epidermodysplasia Verruciformis | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0400966 | Non-alcoholic Fatty Liver Disease | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0010068 | Coronary heart disease | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0281361 | Adenocarcinoma of pancreas | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C1261473 | Sarcoma | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0033575 | Prostatic Diseases | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0029172 | Oral Submucous Fibrosis | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0279702 | Conventional (Clear Cell) Renal Cell Carcinoma | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0014859 | Esophageal Neoplasms | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0265950 | Venous malformation | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C2711227 | Steatohepatitis | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0017636 | Glioblastoma | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0030567 | Parkinson Disease | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
