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 |
---|---|---|---|---|---|
C0031117 | Peripheral Neuropathy | ACOT7 | 11332 | acyl-CoA thioesterase 7 | O00154 |
C0024537 | Malaria, Vivax | ACOT7 | 11332 | acyl-CoA thioesterase 7 | O00154 |
C1306759 | Eosinophilic disorder | ACOT7 | 11332 | acyl-CoA thioesterase 7 | O00154 |
C0948008 | Ischemic stroke | ACOT4 | 122970 | acyl-CoA thioesterase 4 | Q8N9L9 |
C0151744 | Myocardial Ischemia | ACOT2 | 10965 | acyl-CoA thioesterase 2 | P49753 |
C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | ACOT2 | 10965 | acyl-CoA thioesterase 2 | P49753 |
C0023903 | Liver neoplasms | ACOT12 | 134526 | acyl-CoA thioesterase 12 | Q8WYK0 |
C2239176 | Liver carcinoma | ACOT12 | 134526 | acyl-CoA thioesterase 12 | Q8WYK0 |
C0024620 | Primary Malignant Liver Neoplasm | ACOT12 | 134526 | acyl-CoA thioesterase 12 | Q8WYK0 |
C0345904 | Malignant neoplasm of liver | ACOT12 | 134526 | acyl-CoA thioesterase 12 | Q8WYK0 |
C1858991 | Childhood Ataxia with Central Nervous System Hypomyelinization | ACOT12 | 134526 | acyl-CoA thioesterase 12 | Q8WYK0 |
C0023520 | Leukodystrophy | ACOT12 | 134526 | acyl-CoA thioesterase 12 | Q8WYK0 |
C0854795 | Resectable Malignant Liver Neoplasm | ACOT12 | 134526 | acyl-CoA thioesterase 12 | Q8WYK0 |
C0023903 | Liver neoplasms | ACOT1 | 641371 | acyl-CoA thioesterase 1 | Q86TX2 |
C0345904 | Malignant neoplasm of liver | ACOT1 | 641371 | acyl-CoA thioesterase 1 | Q86TX2 |
C0278701 | Gastric Adenocarcinoma | ACOT1 | 641371 | acyl-CoA thioesterase 1 | Q86TX2 |
C0027651 | Neoplasms | ACSS3 | 79611 | acyl-CoA synthetase short chain family member 3 | Q9H6R3 |
C0699791 | Stomach Carcinoma | ACSS3 | 79611 | acyl-CoA synthetase short chain family member 3 | Q9H6R3 |
C0006826 | Malignant Neoplasms | ACSS3 | 79611 | acyl-CoA synthetase short chain family member 3 | Q9H6R3 |
C1306459 | Primary malignant neoplasm | ACSS3 | 79611 | acyl-CoA synthetase short chain family member 3 | Q9H6R3 |
C2239176 | Liver carcinoma | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0265706 | Gastroschisis | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0010051 | Coronary Aneurysm | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C1704436 | Peripheral Arterial Diseases | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0023281 | Leishmaniasis | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
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Last updated: August 19, 2024