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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 ▲ |
|---|---|---|---|---|---|
| C1269683 | Major Depressive Disorder | PARP14 | 54625 | poly(ADP-ribose) polymerase family member 14 | Q460N5 |
| C0006826 | Malignant Neoplasms | PARP14 | 54625 | poly(ADP-ribose) polymerase family member 14 | Q460N5 |
| C0041696 | Unipolar Depression | PARP14 | 54625 | poly(ADP-ribose) polymerase family member 14 | Q460N5 |
| C0004096 | Asthma | PARP14 | 54625 | poly(ADP-ribose) polymerase family member 14 | Q460N5 |
| C0235974 | Pancreatic carcinoma | PARP14 | 54625 | poly(ADP-ribose) polymerase family member 14 | Q460N5 |
| C1332201 | Adult Diffuse Large B-Cell Lymphoma | PARP14 | 54625 | poly(ADP-ribose) polymerase family member 14 | Q460N5 |
| C2239176 | Liver carcinoma | PARP14 | 54625 | poly(ADP-ribose) polymerase family member 14 | Q460N5 |
| C2239176 | Liver carcinoma | FUT11 | 170384 | fucosyltransferase 11 | Q495W5 |
| C0036341 | Schizophrenia | FUT11 | 170384 | fucosyltransferase 11 | Q495W5 |
| C0279702 | Conventional (Clear Cell) Renal Cell Carcinoma | FUT11 | 170384 | fucosyltransferase 11 | Q495W5 |
| C0684249 | Carcinoma of lung | FUT11 | 170384 | fucosyltransferase 11 | Q495W5 |
| C0242379 | Malignant neoplasm of lung | FUT11 | 170384 | fucosyltransferase 11 | Q495W5 |
| C0036572 | Seizures | NRN1L | 123904 | neuritin 1 like | Q496H8 |
| C0037369 | Smoking | GALNTL6 | 442117 | polypeptide N-acetylgalactosaminyltransferase like 6 | Q49A17 |
| C0149745 | Oral Ulcer | GTDC1 | 79712 | glycosyltransferase like domain containing 1 | Q4AE62 |
| C0036341 | Schizophrenia | GTDC1 | 79712 | glycosyltransferase like domain containing 1 | Q4AE62 |
| C0002395 | Alzheimer's Disease | GTDC1 | 79712 | glycosyltransferase like domain containing 1 | Q4AE62 |
| C3280314 | Combined Malonic and Methylmalonic Aciduria | ACSF3 | 197322 | acyl-CoA synthetase family member 3 | Q4G176 |
| C0013421 | Dystonia | ACSF3 | 197322 | acyl-CoA synthetase family member 3 | Q4G176 |
| C0268583 | Methylmalonic acidemia | ACSF3 | 197322 | acyl-CoA synthetase family member 3 | Q4G176 |
| C0024299 | Lymphoma | ACSF3 | 197322 | acyl-CoA synthetase family member 3 | Q4G176 |
| C0011991 | Diarrhea | ACSF3 | 197322 | acyl-CoA synthetase family member 3 | Q4G176 |
| C0025521 | Inborn Errors of Metabolism | ACSF3 | 197322 | acyl-CoA synthetase family member 3 | Q4G176 |
| C0085584 | Encephalopathies | ACSF3 | 197322 | acyl-CoA synthetase family member 3 | Q4G176 |
| C0020615 | Hypoglycemia | ACSF3 | 197322 | acyl-CoA synthetase family member 3 | Q4G176 |
