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 |
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DisGeNET | July 29, 2024 |
Disease ID | Disease Name | Gene Symbol ▼ | Gene ID | Gene Name | UniProt ID |
---|---|---|---|---|---|
C0948008 | Ischemic stroke | CYP1A1 | 1543 | cytochrome P450 family 1 subfamily A member 1 | P04798 |
C0262584 | Carcinoma, Small Cell | CYP1A1 | 1543 | cytochrome P450 family 1 subfamily A member 1 | P04798 |
C0278510 | Childhood Medulloblastoma | CYP1A1 | 1543 | cytochrome P450 family 1 subfamily A member 1 | P04798 |
C0085293 | Hepatitis E | CYP1A1 | 1543 | cytochrome P450 family 1 subfamily A member 1 | P04798 |
C0346647 | Malignant neoplasm of pancreas | CYP1A1 | 1543 | cytochrome P450 family 1 subfamily A member 1 | P04798 |
C0162820 | Dermatitis, Allergic Contact | CYP1A1 | 1543 | cytochrome P450 family 1 subfamily A member 1 | P04798 |
C0085435 | Arthritis, Reactive | CYP1A1 | 1543 | cytochrome P450 family 1 subfamily A member 1 | P04798 |
C0003850 | Arteriosclerosis | CYP1A1 | 1543 | cytochrome P450 family 1 subfamily A member 1 | P04798 |
C0011849 | Diabetes Mellitus | CYP1A1 | 1543 | cytochrome P450 family 1 subfamily A member 1 | P04798 |
C0206624 | Hepatoblastoma | CYP1A1 | 1543 | cytochrome P450 family 1 subfamily A member 1 | P04798 |
C0400966 | Non-alcoholic Fatty Liver Disease | CYP1A1 | 1543 | cytochrome P450 family 1 subfamily A member 1 | P04798 |
C0018671 | Head and Neck Neoplasms | CYP1A1 | 1543 | cytochrome P450 family 1 subfamily A member 1 | P04798 |
C0023530 | Leukopenia | CYP1A1 | 1543 | cytochrome P450 family 1 subfamily A member 1 | P04798 |
C0855197 | Malignant Testicular Germ Cell Tumor | CYP1A1 | 1543 | cytochrome P450 family 1 subfamily A member 1 | P04798 |
C0023890 | Liver Cirrhosis | CYP1A1 | 1543 | cytochrome P450 family 1 subfamily A member 1 | P04798 |
C4552100 | Lynch Syndrome | CYP1A1 | 1543 | cytochrome P450 family 1 subfamily A member 1 | P04798 |
C0004779 | Basal Cell Nevus Syndrome | CYP1A1 | 1543 | cytochrome P450 family 1 subfamily A member 1 | P04798 |
C0264490 | Acute respiratory failure | CYP1A1 | 1543 | cytochrome P450 family 1 subfamily A member 1 | P04798 |
C0031106 | Aggressive Periodontitis | CYP1A1 | 1543 | cytochrome P450 family 1 subfamily A member 1 | P04798 |
C0023532 | Leukoplakia, Oral | CYP1A1 | 1543 | cytochrome P450 family 1 subfamily A member 1 | P04798 |
C0009405 | Hereditary Nonpolyposis Colorectal Neoplasms | CYP1A1 | 1543 | cytochrome P450 family 1 subfamily A member 1 | P04798 |
C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | CYP1A1 | 1543 | cytochrome P450 family 1 subfamily A member 1 | P04798 |
C3203102 | Idiopathic pulmonary arterial hypertension | CYP1A1 | 1543 | cytochrome P450 family 1 subfamily A member 1 | P04798 |
C0028754 | Obesity | CYP1A1 | 1543 | cytochrome P450 family 1 subfamily A member 1 | P04798 |
C0002874 | Aplastic Anemia | CYP1A1 | 1543 | cytochrome P450 family 1 subfamily A member 1 | P04798 |
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Last updated: August 19, 2024