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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 ▼ |
|---|---|---|---|---|---|
| C0009402 | Colorectal Carcinoma | SIGLEC6 | 946 | sialic acid binding Ig like lectin 6 | O43699 |
| C0023434 | Chronic Lymphocytic Leukemia | SIGLEC6 | 946 | sialic acid binding Ig like lectin 6 | O43699 |
| C0242380 | Libman-Sacks Disease | SIGLEC6 | 946 | sialic acid binding Ig like lectin 6 | O43699 |
| C0007137 | Squamous cell carcinoma | PLPP2 | 8612 | phospholipid phosphatase 2 | O43688 |
| C0027651 | Neoplasms | PLPP2 | 8612 | phospholipid phosphatase 2 | O43688 |
| C0007097 | Carcinoma | PLPP2 | 8612 | phospholipid phosphatase 2 | O43688 |
| C4551686 | Malignant neoplasm of soft tissue | PLPP2 | 8612 | phospholipid phosphatase 2 | O43688 |
| C0006826 | Malignant Neoplasms | PLPP2 | 8612 | phospholipid phosphatase 2 | O43688 |
| C1306459 | Primary malignant neoplasm | PLPP2 | 8612 | phospholipid phosphatase 2 | O43688 |
| C0036341 | Schizophrenia | CHST10 | 9486 | carbohydrate sulfotransferase 10 | O43529 |
| C0011311 | Dengue Fever | CHST10 | 9486 | carbohydrate sulfotransferase 10 | O43529 |
| C3150412 | MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 | B4GAT1 | 11041 | beta-1,4-glucuronyltransferase 1 | O43505 |
| C4284790 | Muscular Dystrophy-Dystroglycanopathy (Congenital with Brain and Eye Anomalies) Type A, 1 | B4GAT1 | 11041 | beta-1,4-glucuronyltransferase 1 | O43505 |
| C3150415 | MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 | B4GAT1 | 11041 | beta-1,4-glucuronyltransferase 1 | O43505 |
| C0006142 | Malignant neoplasm of breast | B4GAT1 | 11041 | beta-1,4-glucuronyltransferase 1 | O43505 |
| C1836373 | MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2K | B4GAT1 | 11041 | beta-1,4-glucuronyltransferase 1 | O43505 |
| C3809042 | MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 13 | B4GAT1 | 11041 | beta-1,4-glucuronyltransferase 1 | O43505 |
| C2875316 | Myotubular (centronuclear) myopathy | B4GAT1 | 11041 | beta-1,4-glucuronyltransferase 1 | O43505 |
| C0546264 | Congenital Fiber Type Disproportion | B4GAT1 | 11041 | beta-1,4-glucuronyltransferase 1 | O43505 |
| C0002902 | Anencephaly | B4GAT1 | 11041 | beta-1,4-glucuronyltransferase 1 | O43505 |
| C0456909 | Blindness | B4GAT1 | 11041 | beta-1,4-glucuronyltransferase 1 | O43505 |
| C0265221 | Walker-Warburg congenital muscular dystrophy | B4GAT1 | 11041 | beta-1,4-glucuronyltransferase 1 | O43505 |
| C0266483 | Pachygyria | B4GAT1 | 11041 | beta-1,4-glucuronyltransferase 1 | O43505 |
| C3150416 | MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2 | B4GAT1 | 11041 | beta-1,4-glucuronyltransferase 1 | O43505 |
| C4015184 | MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 12 | B4GAT1 | 11041 | beta-1,4-glucuronyltransferase 1 | O43505 |
