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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 ▲ |
|---|---|---|---|---|---|
| C0014544 | Epilepsy | PIGN | 23556 | phosphatidylinositol glycan anchor biosynthesis class N | O95427 |
| C0266174 | Duodenal atresia | PIGN | 23556 | phosphatidylinositol glycan anchor biosynthesis class N | O95427 |
| C0376480 | Gingival Overgrowth | PIGN | 23556 | phosphatidylinositol glycan anchor biosynthesis class N | O95427 |
| C1368019 | Paget Disease | PIGN | 23556 | phosphatidylinositol glycan anchor biosynthesis class N | O95427 |
| C0023467 | Leukemia, Myelocytic, Acute | PIGN | 23556 | phosphatidylinositol glycan anchor biosynthesis class N | O95427 |
| C0410422 | Chronic multifocal osteomyelitis | PIGN | 23556 | phosphatidylinositol glycan anchor biosynthesis class N | O95427 |
| C0009402 | Colorectal Carcinoma | PIGN | 23556 | phosphatidylinositol glycan anchor biosynthesis class N | O95427 |
| C0235946 | Cerebral atrophy | PIGN | 23556 | phosphatidylinositol glycan anchor biosynthesis class N | O95427 |
| C0265219 | Miller Dieker syndrome | PIGN | 23556 | phosphatidylinositol glycan anchor biosynthesis class N | O95427 |
| C0003466 | Anus, Imperforate | PIGN | 23556 | phosphatidylinositol glycan anchor biosynthesis class N | O95427 |
| C0848558 | Hypospadias | PIGN | 23556 | phosphatidylinositol glycan anchor biosynthesis class N | O95427 |
| C0042580 | Vesico-Ureteral Reflux | PIGN | 23556 | phosphatidylinositol glycan anchor biosynthesis class N | O95427 |
| C0019569 | Hirschsprung Disease | PIGN | 23556 | phosphatidylinositol glycan anchor biosynthesis class N | O95427 |
| C0152013 | Adenocarcinoma of lung (disorder) | PIGN | 23556 | phosphatidylinositol glycan anchor biosynthesis class N | O95427 |
| C0010964 | Dandy-Walker Syndrome | PIGN | 23556 | phosphatidylinositol glycan anchor biosynthesis class N | O95427 |
| C0079541 | Holoprosencephaly | PIGN | 23556 | phosphatidylinositol glycan anchor biosynthesis class N | O95427 |
| C3203102 | Idiopathic pulmonary arterial hypertension | PIGN | 23556 | phosphatidylinositol glycan anchor biosynthesis class N | O95427 |
| C0002418 | Amblyopia | PIGN | 23556 | phosphatidylinositol glycan anchor biosynthesis class N | O95427 |
| C3536714 | Renal dysplasia | PIGN | 23556 | phosphatidylinositol glycan anchor biosynthesis class N | O95427 |
| C3463824 | MYELODYSPLASTIC SYNDROME | PIGN | 23556 | phosphatidylinositol glycan anchor biosynthesis class N | O95427 |
| C0018817 | Atrial Septal Defects | TGDS | 23483 | TDP-glucose 4,6-dehydratase | O95455 |
| C0271441 | Chronic otitis media | TGDS | 23483 | TDP-glucose 4,6-dehydratase | O95455 |
| C0019294 | Hernia, Inguinal | TGDS | 23483 | TDP-glucose 4,6-dehydratase | O95455 |
| C0344315 | Depressed mood | TGDS | 23483 | TDP-glucose 4,6-dehydratase | O95455 |
| C0011581 | Depressive disorder | TGDS | 23483 | TDP-glucose 4,6-dehydratase | O95455 |
