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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 |
|---|---|---|---|---|---|
| C0010068 | Coronary heart disease | IL1RL1 | 9173 | interleukin 1 receptor like 1 | Q01638 |
| C0023343 | Leprosy | IL1RL1 | 9173 | interleukin 1 receptor like 1 | Q01638 |
| C0036329 | Schistosomiasis japonica | IL1RL1 | 9173 | interleukin 1 receptor like 1 | Q01638 |
| C1449563 | Cardiomyopathy, Familial Idiopathic | IL1RL1 | 9173 | interleukin 1 receptor like 1 | Q01638 |
| C0004364 | Autoimmune Diseases | IL1RL1 | 9173 | interleukin 1 receptor like 1 | Q01638 |
| C0341106 | Eosinophilic esophagitis | IL1RL1 | 9173 | interleukin 1 receptor like 1 | Q01638 |
| C1332977 | Childhood Leukemia | IL1RL1 | 9173 | interleukin 1 receptor like 1 | Q01638 |
| C0019163 | Hepatitis B | IL1RL1 | 9173 | interleukin 1 receptor like 1 | Q01638 |
| C0340076 | Asthmatic pulmonary eosinophilia | IL1RL1 | 9173 | interleukin 1 receptor like 1 | Q01638 |
| C0023452 | Childhood Acute Lymphoblastic Leukemia | IL1RL1 | 9173 | interleukin 1 receptor like 1 | Q01638 |
| C0024117 | Chronic Obstructive Airway Disease | IL1RL1 | 9173 | interleukin 1 receptor like 1 | Q01638 |
| C0011854 | Diabetes Mellitus, Insulin-Dependent | IL1RL1 | 9173 | interleukin 1 receptor like 1 | Q01638 |
| C2607914 | Allergic rhinitis (disorder) | IL1RL1 | 9173 | interleukin 1 receptor like 1 | Q01638 |
| C0010314 | Cri-du-Chat Syndrome | IL1RL1 | 9173 | interleukin 1 receptor like 1 | Q01638 |
| C0018801 | Heart failure | IL1RL1 | 9173 | interleukin 1 receptor like 1 | Q01638 |
| C1708371 | Histiocytoid Cardiomyopathy | IL1RL1 | 9173 | interleukin 1 receptor like 1 | Q01638 |
| C0018799 | Heart Diseases | IL1RL1 | 9173 | interleukin 1 receptor like 1 | Q01638 |
| C4317295 | Congenital disorder of glycosylation type 1s | RFT1 | 91869 | RFT1 homolog | Q96AA3 |
| C0036572 | Seizures | RFT1 | 91869 | RFT1 homolog | Q96AA3 |
| C0018784 | Sensorineural Hearing Loss (disorder) | RFT1 | 91869 | RFT1 homolog | Q96AA3 |
| C0011849 | Diabetes Mellitus | RFT1 | 91869 | RFT1 homolog | Q96AA3 |
| C0025958 | Microcephaly | RFT1 | 91869 | RFT1 homolog | Q96AA3 |
| C0013336 | Dwarfism | RFT1 | 91869 | RFT1 homolog | Q96AA3 |
| C2677590 | Congenital Disorder Of Glycosylation, Type In | RFT1 | 91869 | RFT1 homolog | Q96AA3 |
| C3665347 | Visual Impairment | RFT1 | 91869 | RFT1 homolog | Q96AA3 |
