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 |
---|---|---|---|---|---|
C0155877 | Allergic asthma | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
C0034735 | Raynaud Phenomenon | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
C0004153 | Atherosclerosis | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
C0020071 | Hereditary Sensory Autonomic Neuropathy, Type 1 | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
C0035078 | Kidney Failure | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
C0162311 | Androgenetic Alopecia | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
C0021775 | Intermittent Claudication | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
C0020500 | Hyperoxaluria | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
C0011603 | Dermatitis | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
C0042109 | Urticaria | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
C0004245 | Atrioventricular Block | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
C0004096 | Asthma | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
C0221232 | Welts | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
C0027709 | Nephrocalcinosis | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
C0392525 | Nephrolithiasis | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
C0268646 | Isolated cystinuria | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
C4721453 | Peripheral Nervous System Diseases | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
C0013595 | Eczema | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
C0017636 | Glioblastoma | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
C0018889 | Helminthiasis | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
C0264995 | Occlusion of artery (disorder) | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
C0014122 | Subacute Bacterial Endocarditis | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
C1561643 | Chronic Kidney Diseases | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
C0279980 | Extra-osseous Ewing's sarcoma | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
C0025517 | Metabolic Diseases | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
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Last updated: August 19, 2024