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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 |
|---|---|---|---|---|---|
| C0243026 | Sepsis | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0003850 | Arteriosclerosis | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0029456 | Osteoporosis | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0740391 | Middle Cerebral Artery Occlusion | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0030305 | Pancreatitis | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0406500 | Lipodermatosclerosis | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0027051 | Myocardial Infarction | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0032285 | Pneumonia | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0011847 | Diabetes | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0035344 | Retinopathy of Prematurity | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0007222 | Cardiovascular Diseases | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0027697 | Nephritis | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C1306459 | Primary malignant neoplasm | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0007785 | Cerebral Infarction | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C4721610 | Carcinoma, Ovarian Epithelial | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0024121 | Lung Neoplasms | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0042373 | Vascular Diseases | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0018802 | Congestive heart failure | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0004114 | Astrocytoma | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0699790 | Colon Carcinoma | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0018799 | Heart Diseases | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0018021 | Goiter | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0238463 | Papillary thyroid carcinoma | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0006118 | Brain Neoplasms | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
