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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 ▼ |
|---|---|---|---|---|---|
| C0023890 | Liver Cirrhosis | CYP2R1 | 120227 | cytochrome P450 family 2 subfamily R member 1 | Q6VVX0 |
| C0279702 | Conventional (Clear Cell) Renal Cell Carcinoma | CYP2R1 | 120227 | cytochrome P450 family 2 subfamily R member 1 | Q6VVX0 |
| C0027709 | Nephrocalcinosis | CYP2R1 | 120227 | cytochrome P450 family 2 subfamily R member 1 | Q6VVX0 |
| C0010054 | Coronary Arteriosclerosis | CYP2R1 | 120227 | cytochrome P450 family 2 subfamily R member 1 | Q6VVX0 |
| C4721806 | Carcinoma, Basal Cell | CYP2R1 | 120227 | cytochrome P450 family 2 subfamily R member 1 | Q6VVX0 |
| C0042170 | Uveomeningoencephalitic Syndrome | CYP2R1 | 120227 | cytochrome P450 family 2 subfamily R member 1 | Q6VVX0 |
| C0003873 | Rheumatoid Arthritis | CYP2R1 | 120227 | cytochrome P450 family 2 subfamily R member 1 | Q6VVX0 |
| C1956346 | Coronary Artery Disease | CYP2R1 | 120227 | cytochrome P450 family 2 subfamily R member 1 | Q6VVX0 |
| C0085682 | Hypophosphatemia | CYP2R1 | 120227 | cytochrome P450 family 2 subfamily R member 1 | Q6VVX0 |
| C0151744 | Myocardial Ischemia | CYP2R1 | 120227 | cytochrome P450 family 2 subfamily R member 1 | Q6VVX0 |
| C0039621 | Tetany | CYP2R1 | 120227 | cytochrome P450 family 2 subfamily R member 1 | Q6VVX0 |
| C0028960 | Oligospermia | CYP2R1 | 120227 | cytochrome P450 family 2 subfamily R member 1 | Q6VVX0 |
| C0400966 | Non-alcoholic Fatty Liver Disease | CYP2R1 | 120227 | cytochrome P450 family 2 subfamily R member 1 | Q6VVX0 |
| C0235974 | Pancreatic carcinoma | CYP2R1 | 120227 | cytochrome P450 family 2 subfamily R member 1 | Q6VVX0 |
| C0019163 | Hepatitis B | CYP2R1 | 120227 | cytochrome P450 family 2 subfamily R member 1 | Q6VVX0 |
| C3887650 | Adult Rickets | CYP2R1 | 120227 | cytochrome P450 family 2 subfamily R member 1 | Q6VVX0 |
| C3887461 | Head and Neck Carcinoma | CYP2R1 | 120227 | cytochrome P450 family 2 subfamily R member 1 | Q6VVX0 |
| C0524620 | Metabolic Syndrome X | CYP2R1 | 120227 | cytochrome P450 family 2 subfamily R member 1 | Q6VVX0 |
| C0948008 | Ischemic stroke | CYP2R1 | 120227 | cytochrome P450 family 2 subfamily R member 1 | Q6VVX0 |
| C0004153 | Atherosclerosis | CLEC9A | 283420 | C-type lectin domain containing 9A | Q6UXN8 |
| C0042769 | Virus Diseases | CLEC9A | 283420 | C-type lectin domain containing 9A | Q6UXN8 |
| C0027651 | Neoplasms | CLEC9A | 283420 | C-type lectin domain containing 9A | Q6UXN8 |
| C3714636 | Pneumonitis | CLEC9A | 283420 | C-type lectin domain containing 9A | Q6UXN8 |
| C0041296 | Tuberculosis | CLEC9A | 283420 | C-type lectin domain containing 9A | Q6UXN8 |
| C0001175 | Acquired Immunodeficiency Syndrome | CLEC9A | 283420 | C-type lectin domain containing 9A | Q6UXN8 |
