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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 |
|---|---|---|---|---|---|
| C0344315 | Depressed mood | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0009402 | Colorectal Carcinoma | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0011847 | Diabetes | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0268353 | Cutis laxa, x-linked | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0006826 | Malignant Neoplasms | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0006142 | Malignant neoplasm of breast | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0376358 | Malignant neoplasm of prostate | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0011849 | Diabetes Mellitus | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0020456 | Hyperglycemia | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0026705 | Mucopolysaccharidosis II | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0021933 | Intussusception | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0004352 | Autistic Disorder | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0011581 | Depressive disorder | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0151744 | Myocardial Ischemia | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0023418 | leukemia | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0563625 | Agnosia for Pain | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C1306459 | Primary malignant neoplasm | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0014544 | Epilepsy | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0019061 | Hemolytic-Uremic Syndrome | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0678222 | Breast Carcinoma | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0206624 | Hepatoblastoma | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0032460 | Polycystic Ovary Syndrome | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C0023467 | Leukemia, Myelocytic, Acute | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
| C1834582 | MYELOPROLIFERATIVE SYNDROME, TRANSIENT | SLC35G1 | 159371 | solute carrier family 35 member G1 | Q2M3R5 |
