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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 |
|---|---|---|---|---|---|
| C0042164 | Uveitis | RTN4R | 65078 | reticulon 4 receptor | Q9BZR6 |
| C0280803 | Primary central nervous system lymphoma | RTN4R | 65078 | reticulon 4 receptor | Q9BZR6 |
| C0011849 | Diabetes Mellitus | RTN4R | 65078 | reticulon 4 receptor | Q9BZR6 |
| C1332977 | Childhood Leukemia | RTN4R | 65078 | reticulon 4 receptor | Q9BZR6 |
| C0007137 | Squamous cell carcinoma | RTN4R | 65078 | reticulon 4 receptor | Q9BZR6 |
| C0029134 | Optic Neuritis | RTN4R | 65078 | reticulon 4 receptor | Q9BZR6 |
| C2931822 | Nasopharyngeal carcinoma | RTN4R | 65078 | reticulon 4 receptor | Q9BZR6 |
| C0079588 | Ichthyosis, X-Linked | RTN4R | 65078 | reticulon 4 receptor | Q9BZR6 |
| C0007682 | CNS disorder | RTN4R | 65078 | reticulon 4 receptor | Q9BZR6 |
| C0153633 | Malignant neoplasm of brain | RTN4R | 65078 | reticulon 4 receptor | Q9BZR6 |
| C0023418 | leukemia | RTN4R | 65078 | reticulon 4 receptor | Q9BZR6 |
| C0152013 | Adenocarcinoma of lung (disorder) | RTN4R | 65078 | reticulon 4 receptor | Q9BZR6 |
| C1319315 | Adenocarcinoma of large intestine | RTN4R | 65078 | reticulon 4 receptor | Q9BZR6 |
| C0149925 | Small cell carcinoma of lung | RTN4R | 65078 | reticulon 4 receptor | Q9BZR6 |
| C2931822 | Nasopharyngeal carcinoma | RTN4RL1 | 146760 | reticulon 4 receptor like 1 | Q86UN2 |
| C0152021 | Congenital heart disease | RTN4RL1 | 146760 | reticulon 4 receptor like 1 | Q86UN2 |
| C0023467 | Leukemia, Myelocytic, Acute | RTN4RL1 | 146760 | reticulon 4 receptor like 1 | Q86UN2 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | RTN4RL1 | 146760 | reticulon 4 receptor like 1 | Q86UN2 |
| C0009402 | Colorectal Carcinoma | RTN4RL2 | 349667 | reticulon 4 receptor like 2 | Q86UN3 |
| C0010964 | Dandy-Walker Syndrome | RXYLT1 | 10329 | ribitol xylosyltransferase 1 | Q9Y2B1 |
| C0266483 | Pachygyria | RXYLT1 | 10329 | ribitol xylosyltransferase 1 | Q9Y2B1 |
| C0029124 | Optic Atrophy | RXYLT1 | 10329 | ribitol xylosyltransferase 1 | Q9Y2B1 |
| C3554381 | MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 10 | RXYLT1 | 10329 | ribitol xylosyltransferase 1 | Q9Y2B1 |
| C0265221 | Walker-Warburg congenital muscular dystrophy | RXYLT1 | 10329 | ribitol xylosyltransferase 1 | Q9Y2B1 |
| C3714756 | Intellectual Disability | RXYLT1 | 10329 | ribitol xylosyltransferase 1 | Q9Y2B1 |
