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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 |
|---|---|---|---|---|---|
| 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 |
| C0036341 | Schizophrenia | DGKI | 9162 | diacylglycerol kinase iota | O75912 |
| C0476254 | Dyslexia | DGKI | 9162 | diacylglycerol kinase iota | O75912 |
| C1621958 | Glioblastoma Multiforme | DGKI | 9162 | diacylglycerol kinase iota | O75912 |
| C0013537 | Eclampsia | DGKI | 9162 | diacylglycerol kinase iota | O75912 |
| C0001175 | Acquired Immunodeficiency Syndrome | DGKI | 9162 | diacylglycerol kinase iota | O75912 |
| C0025202 | melanoma | DGKI | 9162 | diacylglycerol kinase iota | O75912 |
| C0027651 | Neoplasms | DGKI | 9162 | diacylglycerol kinase iota | O75912 |
| C0278878 | Adult Glioblastoma | DGKI | 9162 | diacylglycerol kinase iota | O75912 |
| C0017636 | Glioblastoma | DGKI | 9162 | diacylglycerol kinase iota | O75912 |
| C2239176 | Liver carcinoma | UAP1L1 | 91373 | UDP-N-acetylglucosamine pyrophosphorylase 1 like 1 | Q3KQV9 |
| C0023903 | Liver neoplasms | UAP1L1 | 91373 | UDP-N-acetylglucosamine pyrophosphorylase 1 like 1 | Q3KQV9 |
| C0005741 | Blepharitis | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
| C3714756 | Intellectual Disability | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
| C0235833 | Congenital diaphragmatic hernia | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
| C1853099 | Cornelia de Lange Syndrome 3 | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
| C0270972 | Cornelia De Lange Syndrome | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
| C0024299 | Lymphoma | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
| C0019294 | Hernia, Inguinal | SMC3 | 9126 | structural maintenance of chromosomes 3 | Q9UQE7 |
