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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 |
|---|---|---|---|---|---|
| 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 |
| C0034013 | Precocious Puberty | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0028738 | Nystagmus | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0019196 | Hepatitis C | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0019163 | Hepatitis B | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0036857 | Severe intellectual disability | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0015310 | Exotropia | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0022353 | Neonatal Jaundice | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0002895 | Anemia, Sickle Cell | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0038379 | Strabismus | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0010964 | Dandy-Walker Syndrome | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0005283 | beta Thalassemia | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0018784 | Sensorineural Hearing Loss (disorder) | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C1856251 | Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
