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 | CYP4F2 | 8529 | cytochrome P450 family 4 subfamily F member 2 | P78329 |
C0524620 | Metabolic Syndrome X | CYP4F2 | 8529 | cytochrome P450 family 4 subfamily F member 2 | P78329 |
C1861172 | Venous Thromboembolism | CYP4F2 | 8529 | cytochrome P450 family 4 subfamily F member 2 | P78329 |
C1956346 | Coronary Artery Disease | CYP4F2 | 8529 | cytochrome P450 family 4 subfamily F member 2 | P78329 |
C0027051 | Myocardial Infarction | CYP4F2 | 8529 | cytochrome P450 family 4 subfamily F member 2 | P78329 |
C0400966 | Non-alcoholic Fatty Liver Disease | CYP4F2 | 8529 | cytochrome P450 family 4 subfamily F member 2 | P78329 |
C0007785 | Cerebral Infarction | CYP4F2 | 8529 | cytochrome P450 family 4 subfamily F member 2 | P78329 |
C0085580 | Essential Hypertension | CYP4F2 | 8529 | cytochrome P450 family 4 subfamily F member 2 | P78329 |
C0162309 | Adrenoleukodystrophy | CYP4F2 | 8529 | cytochrome P450 family 4 subfamily F member 2 | P78329 |
C1306459 | Primary malignant neoplasm | CYP4F2 | 8529 | cytochrome P450 family 4 subfamily F member 2 | P78329 |
C0004238 | Atrial Fibrillation | CYP4F2 | 8529 | cytochrome P450 family 4 subfamily F member 2 | P78329 |
C0004153 | Atherosclerosis | CYP4F2 | 8529 | cytochrome P450 family 4 subfamily F member 2 | P78329 |
C1335302 | Pancreatic Ductal Adenocarcinoma | CYP4F2 | 8529 | cytochrome P450 family 4 subfamily F member 2 | P78329 |
C0027651 | Neoplasms | CYP4F2 | 8529 | cytochrome P450 family 4 subfamily F member 2 | P78329 |
C0042373 | Vascular Diseases | CYP4F2 | 8529 | cytochrome P450 family 4 subfamily F member 2 | P78329 |
C0007222 | Cardiovascular Diseases | CYP4F2 | 8529 | cytochrome P450 family 4 subfamily F member 2 | P78329 |
C0003850 | Arteriosclerosis | CYP4F2 | 8529 | cytochrome P450 family 4 subfamily F member 2 | P78329 |
C0010054 | Coronary Arteriosclerosis | CYP4F2 | 8529 | cytochrome P450 family 4 subfamily F member 2 | P78329 |
C0010346 | Crohn Disease | CYP4F2 | 8529 | cytochrome P450 family 4 subfamily F member 2 | P78329 |
C0007820 | Cerebrovascular Disorders | CYP4F2 | 8529 | cytochrome P450 family 4 subfamily F member 2 | P78329 |
C0028754 | Obesity | CYP4F2 | 8529 | cytochrome P450 family 4 subfamily F member 2 | P78329 |
C0006826 | Malignant Neoplasms | CYP4F2 | 8529 | cytochrome P450 family 4 subfamily F member 2 | P78329 |
C2751492 | AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED | GPC5 | 2262 | glypican 5 | P78333 |
C0235974 | Pancreatic carcinoma | GPC5 | 2262 | glypican 5 | P78333 |
C1335302 | Pancreatic Ductal Adenocarcinoma | GPC5 | 2262 | glypican 5 | P78333 |
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Last updated: August 19, 2024