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 |
---|---|---|---|---|---|
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 |
C0038454 | Cerebrovascular accident | CYP2J2 | 1573 | cytochrome P450 family 2 subfamily J member 2 | P51589 |
C0010068 | Coronary heart disease | CYP2J2 | 1573 | cytochrome P450 family 2 subfamily J member 2 | P51589 |
C0027651 | Neoplasms | CYP2J2 | 1573 | cytochrome P450 family 2 subfamily J member 2 | P51589 |
C0027051 | Myocardial Infarction | CYP2J2 | 1573 | cytochrome P450 family 2 subfamily J member 2 | P51589 |
C0151744 | Myocardial Ischemia | CYP2J2 | 1573 | cytochrome P450 family 2 subfamily J member 2 | P51589 |
C0598608 | Hyperhomocysteinemia | CYP2J2 | 1573 | cytochrome P450 family 2 subfamily J member 2 | P51589 |
C0004238 | Atrial Fibrillation | CYP2J2 | 1573 | cytochrome P450 family 2 subfamily J member 2 | P51589 |
C0006826 | Malignant Neoplasms | CYP2J2 | 1573 | cytochrome P450 family 2 subfamily J member 2 | P51589 |
C0010054 | Coronary Arteriosclerosis | CYP2J2 | 1573 | cytochrome P450 family 2 subfamily J member 2 | P51589 |
C0018801 | Heart failure | CYP2J2 | 1573 | cytochrome P450 family 2 subfamily J member 2 | P51589 |
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Last updated: August 19, 2024