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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 ▲ |
|---|---|---|---|---|---|
| C0029124 | Optic Atrophy | STT3B | 201595 | STT3 oligosaccharyltransferase complex catalytic subunit B | Q8TCJ2 |
| C0027819 | Neuroblastoma | CERK | 64781 | ceramide kinase | Q8TCT0 |
| C0700095 | Central neuroblastoma | CERK | 64781 | ceramide kinase | Q8TCT0 |
| C0006142 | Malignant neoplasm of breast | CERK | 64781 | ceramide kinase | Q8TCT0 |
| C0028754 | Obesity | CERK | 64781 | ceramide kinase | Q8TCT0 |
| C0678222 | Breast Carcinoma | CERK | 64781 | ceramide kinase | Q8TCT0 |
| C1458155 | Mammary Neoplasms | CERK | 64781 | ceramide kinase | Q8TCT0 |
| C0543918 | SCHIZOPHRENIA 10 | CERK | 64781 | ceramide kinase | Q8TCT0 |
| C0027651 | Neoplasms | CERK | 64781 | ceramide kinase | Q8TCT0 |
| C1832661 | ANOPHTHALMIA AND PULMONARY HYPOPLASIA | CERK | 64781 | ceramide kinase | Q8TCT0 |
| C0009319 | Colitis | CERK | 64781 | ceramide kinase | Q8TCT0 |
| C0036220 | Kaposi Sarcoma | CERK | 64781 | ceramide kinase | Q8TCT0 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | PHOSPHO1 | 162466 | phosphoethanolamine/phosphocholine phosphatase 1 | Q8TCT1 |
| C0029442 | Osteomalacia | PHOSPHO1 | 162466 | phosphoethanolamine/phosphocholine phosphatase 1 | Q8TCT1 |
| C3887650 | Adult Rickets | PHOSPHO1 | 162466 | phosphoethanolamine/phosphocholine phosphatase 1 | Q8TCT1 |
| C0376358 | Malignant neoplasm of prostate | SLC2A12 | 154091 | solute carrier family 2 member 12 | Q8TD20 |
| C0011847 | Diabetes | SLC2A12 | 154091 | solute carrier family 2 member 12 | Q8TD20 |
| C0027651 | Neoplasms | SLC2A12 | 154091 | solute carrier family 2 member 12 | Q8TD20 |
| C0020676 | Hypothyroidism | SLC2A12 | 154091 | solute carrier family 2 member 12 | Q8TD20 |
| C0002726 | Amyloidosis | SLC2A12 | 154091 | solute carrier family 2 member 12 | Q8TD20 |
| C1956346 | Coronary Artery Disease | SLC2A12 | 154091 | solute carrier family 2 member 12 | Q8TD20 |
| C0011854 | Diabetes Mellitus, Insulin-Dependent | SLC2A12 | 154091 | solute carrier family 2 member 12 | Q8TD20 |
| C0026764 | Multiple Myeloma | SLC2A12 | 154091 | solute carrier family 2 member 12 | Q8TD20 |
| C0006142 | Malignant neoplasm of breast | SLC2A12 | 154091 | solute carrier family 2 member 12 | Q8TD20 |
| C0400966 | Non-alcoholic Fatty Liver Disease | SLC2A12 | 154091 | solute carrier family 2 member 12 | Q8TD20 |
