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 |
---|---|---|---|---|---|
C0220756 | Niemann-Pick Disease, Type C | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0020456 | Hyperglycemia | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C2931822 | Nasopharyngeal carcinoma | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0241005 | Creatine phosphokinase serum increased | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0015934 | Fetal Growth Retardation | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0036572 | Seizures | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0524620 | Metabolic Syndrome X | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0021390 | Inflammatory Bowel Diseases | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C3887523 | Very long chain acyl-CoA dehydrogenase deficiency | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0878544 | Cardiomyopathies | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C1956346 | Coronary Artery Disease | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0233794 | Memory impairment | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0268634 | Disorder of fatty acid metabolism | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0206655 | Alveolar rhabdomyosarcoma | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C3888391 | Nonnuclear polymorphic congenital cataract | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0268596 | Multiple Acyl Coenzyme A Dehydrogenase Deficiency | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0024623 | Malignant neoplasm of stomach | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0220994 | Hyperammonemia | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0279626 | Squamous cell carcinoma of esophagus | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0011581 | Depressive disorder | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0699791 | Stomach Carcinoma | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0026769 | Multiple Sclerosis | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0019158 | Hepatitis | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0014544 | Epilepsy | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
C0017636 | Glioblastoma | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
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