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DisGeNET
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 ▲ |
|---|---|---|---|---|---|
| C0006826 | Malignant Neoplasms | MPPE1 | 65258 | metallophosphoesterase 1 | Q53F39 |
| C0005586 | Bipolar Disorder | MPPE1 | 65258 | metallophosphoesterase 1 | Q53F39 |
| C0006012 | Borderline Personality Disorder | MPPE1 | 65258 | metallophosphoesterase 1 | Q53F39 |
| C0019163 | Hepatitis B | MPPE1 | 65258 | metallophosphoesterase 1 | Q53F39 |
| C0021400 | Influenza | MPPE1 | 65258 | metallophosphoesterase 1 | Q53F39 |
| C3714636 | Pneumonitis | MPPE1 | 65258 | metallophosphoesterase 1 | Q53F39 |
| C1266044 | Collecting Duct Carcinoma of the Kidney | MPPE1 | 65258 | metallophosphoesterase 1 | Q53F39 |
| C0024534 | Malaria, Cerebral | MPPE1 | 65258 | metallophosphoesterase 1 | Q53F39 |
| C0025202 | melanoma | MPPE1 | 65258 | metallophosphoesterase 1 | Q53F39 |
| C0024530 | Malaria | MPPE1 | 65258 | metallophosphoesterase 1 | Q53F39 |
| C0004096 | Asthma | ORMDL2 | 29095 | ORMDL sphingolipid biosynthesis regulator 2 | Q53FV1 |
| C0028866 | Oculomotor Nerve Paralysis | ACSM3 | 6296 | acyl-CoA synthetase medium chain family member 3 | Q53FZ2 |
| C0948008 | Ischemic stroke | ACSM3 | 6296 | acyl-CoA synthetase medium chain family member 3 | Q53FZ2 |
| C0020635 | Hypopituitarism | ACSM3 | 6296 | acyl-CoA synthetase medium chain family member 3 | Q53FZ2 |
| C0007785 | Cerebral Infarction | ACSM3 | 6296 | acyl-CoA synthetase medium chain family member 3 | Q53FZ2 |
| C0038454 | Cerebrovascular accident | ACSM3 | 6296 | acyl-CoA synthetase medium chain family member 3 | Q53FZ2 |
| C0007222 | Cardiovascular Diseases | ACSM3 | 6296 | acyl-CoA synthetase medium chain family member 3 | Q53FZ2 |
| C0524620 | Metabolic Syndrome X | ACSM3 | 6296 | acyl-CoA synthetase medium chain family member 3 | Q53FZ2 |
| C0852949 | Arteriopathic disease | ACSM3 | 6296 | acyl-CoA synthetase medium chain family member 3 | Q53FZ2 |
| C0028840 | Ocular Hypertension | ACSM3 | 6296 | acyl-CoA synthetase medium chain family member 3 | Q53FZ2 |
| C0086543 | Cataract | ACSM3 | 6296 | acyl-CoA synthetase medium chain family member 3 | Q53FZ2 |
| C0002871 | Anemia | ACSM3 | 6296 | acyl-CoA synthetase medium chain family member 3 | Q53FZ2 |
| C0917996 | Cerebral Aneurysm | ACSM3 | 6296 | acyl-CoA synthetase medium chain family member 3 | Q53FZ2 |
| C0153633 | Malignant neoplasm of brain | ACSM3 | 6296 | acyl-CoA synthetase medium chain family member 3 | Q53FZ2 |
| C1837461 | SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 | ACSM3 | 6296 | acyl-CoA synthetase medium chain family member 3 | Q53FZ2 |
