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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 |
|---|---|---|---|---|---|
| C4721532 | Lymphoma, Non-Hodgkin, Familial | TMEM260 | 54916 | transmembrane protein 260 | Q9NX78 |
| C0018818 | Ventricular Septal Defects | TMEM260 | 54916 | transmembrane protein 260 | Q9NX78 |
| C0041207 | Truncus Arteriosus, Persistent | TMEM260 | 54916 | transmembrane protein 260 | Q9NX78 |
| C0024305 | Lymphoma, Non-Hodgkin | TMEM260 | 54916 | transmembrane protein 260 | Q9NX78 |
| C1306459 | Primary malignant neoplasm | TMEM260 | 54916 | transmembrane protein 260 | Q9NX78 |
| C0006826 | Malignant Neoplasms | TMEM260 | 54916 | transmembrane protein 260 | Q9NX78 |
| C0001973 | Alcoholic Intoxication, Chronic | TMEM260 | 54916 | transmembrane protein 260 | Q9NX78 |
| C1565489 | Renal Insufficiency | TMEM260 | 54916 | transmembrane protein 260 | Q9NX78 |
| C0023467 | Leukemia, Myelocytic, Acute | TMEM260 | 54916 | transmembrane protein 260 | Q9NX78 |
| C2711227 | Steatohepatitis | TMEM199 | 147007 | transmembrane protein 199 | Q8N511 |
| C4225190 | CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIp | TMEM199 | 147007 | transmembrane protein 199 | Q8N511 |
| C4317295 | Congenital disorder of glycosylation type 1s | TMEM199 | 147007 | transmembrane protein 199 | Q8N511 |
| C0678222 | Breast Carcinoma | TMEM199 | 147007 | transmembrane protein 199 | Q8N511 |
| C0006142 | Malignant neoplasm of breast | TMEM199 | 147007 | transmembrane protein 199 | Q8N511 |
| C0153252 | Systemic candidiasis | TMEM199 | 147007 | transmembrane protein 199 | Q8N511 |
| C0023895 | Liver diseases | TMEM199 | 147007 | transmembrane protein 199 | Q8N511 |
| C0015695 | Fatty Liver | TMEM199 | 147007 | transmembrane protein 199 | Q8N511 |
| C3553571 | Carbohydrate deficient glycoprotein syndrome type 2k | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
| C0575158 | Kyphoscoliosis deformity of spine | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
| C0241005 | Creatine phosphokinase serum increased | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
| C0011989 | Camurati-Engelmann Syndrome | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
| C1306459 | Primary malignant neoplasm | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
| C0002452 | Amelogenesis Imperfecta | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
| C2239176 | Liver carcinoma | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
| C0013336 | Dwarfism | TMEM165 | 55858 | transmembrane protein 165 | Q9HC07 |
