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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 |
|---|---|---|---|---|---|
| C0027651 | Neoplasms | RPE | 6120 | ribulose-5-phosphate-3-epimerase | Q96AT9 |
| C0339510 | Vitelliform Macular Dystrophy | RPE | 6120 | ribulose-5-phosphate-3-epimerase | Q96AT9 |
| C0276289 | Zika Virus Infection | RPE | 6120 | ribulose-5-phosphate-3-epimerase | Q96AT9 |
| C0152439 | Retinoschisis | RPE | 6120 | ribulose-5-phosphate-3-epimerase | Q96AT9 |
| C1832174 | DOYNE HONEYCOMB RETINAL DYSTROPHY | RPE | 6120 | ribulose-5-phosphate-3-epimerase | Q96AT9 |
| C1862382 | SVEINSSON CHORIORETINAL ATROPHY | RPE | 6120 | ribulose-5-phosphate-3-epimerase | Q96AT9 |
| C0034372 | Quadriplegia | RPE | 6120 | ribulose-5-phosphate-3-epimerase | Q96AT9 |
| C0154822 | Serous retinal detachment | RPE | 6120 | ribulose-5-phosphate-3-epimerase | Q96AT9 |
| C0162830 | Dermatitis, Phototoxic | RPE | 6120 | ribulose-5-phosphate-3-epimerase | Q96AT9 |
| C0409818 | Chronic Infantile Neurological, Cutaneous, and Articular Syndrome | RPE | 6120 | ribulose-5-phosphate-3-epimerase | Q96AT9 |
| C0279000 | Liver and Intrahepatic Biliary Tract Carcinoma | RPE | 6120 | ribulose-5-phosphate-3-epimerase | Q96AT9 |
| C0345904 | Malignant neoplasm of liver | RPE | 6120 | ribulose-5-phosphate-3-epimerase | Q96AT9 |
| C0154830 | Proliferative diabetic retinopathy | RPE | 6120 | ribulose-5-phosphate-3-epimerase | Q96AT9 |
| C0015397 | Disorder of eye | RPE | 6120 | ribulose-5-phosphate-3-epimerase | Q96AT9 |
| C0339535 | Night blindness, congenital stationary | NYX | 60506 | nyctalopin | Q9GZU5 |
| C1848172 | NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A | NYX | 60506 | nyctalopin | Q9GZU5 |
| C0038379 | Strabismus | NYX | 60506 | nyctalopin | Q9GZU5 |
| C0028077 | Nyctalopia | NYX | 60506 | nyctalopin | Q9GZU5 |
| C3495587 | Night Blindness, Congenital Stationary, Type 1A | NYX | 60506 | nyctalopin | Q9GZU5 |
| C0035309 | Retinal Diseases | NYX | 60506 | nyctalopin | Q9GZU5 |
| C0007682 | CNS disorder | NYX | 60506 | nyctalopin | Q9GZU5 |
| C0027092 | Myopia | NYX | 60506 | nyctalopin | Q9GZU5 |
| C0023418 | leukemia | NYX | 60506 | nyctalopin | Q9GZU5 |
| C0152200 | Achromatopsia | NYX | 60506 | nyctalopin | Q9GZU5 |
| C0015397 | Disorder of eye | NYX | 60506 | nyctalopin | Q9GZU5 |
