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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 |
|---|---|---|---|---|---|
| C1636149 | Macular dystrophy, corneal type 1 | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0002395 | Alzheimer's Disease | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0002875 | Cooley's anemia | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C1527366 | Salaam Seizures | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0014859 | Esophageal Neoplasms | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0221023 | Cyclic neutropenia | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0152018 | Esophageal carcinoma | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0013336 | Dwarfism | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0003081 | Anisometropia | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0524620 | Metabolic Syndrome X | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0400966 | Non-alcoholic Fatty Liver Disease | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0857007 | Hyperbilirubinemia, Neonatal | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C4721610 | Carcinoma, Ovarian Epithelial | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0376358 | Malignant neoplasm of prostate | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0014877 | Esotropia | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0011226 | Hepatitis D Infection | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0036572 | Seizures | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0919267 | ovarian neoplasm | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0034194 | Pyloric Stenosis | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0271979 | Thalassemia Intermedia | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0600139 | Prostate carcinoma | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0010278 | Craniosynostosis | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C4317295 | Congenital disorder of glycosylation type 1s | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C1140680 | Malignant neoplasm of ovary | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C1332206 | Adult Lymphoma | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
