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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 ▼ |
|---|---|---|---|---|---|
| C0023467 | Leukemia, Myelocytic, Acute | CHST9 | 83539 | carbohydrate sulfotransferase 9 | Q7L1S5 |
| C1269683 | Major Depressive Disorder | CHST9 | 83539 | carbohydrate sulfotransferase 9 | Q7L1S5 |
| C1956346 | Coronary Artery Disease | CHST9 | 83539 | carbohydrate sulfotransferase 9 | Q7L1S5 |
| C0678222 | Breast Carcinoma | CHST9 | 83539 | carbohydrate sulfotransferase 9 | Q7L1S5 |
| C1837461 | SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 | CHST9 | 83539 | carbohydrate sulfotransferase 9 | Q7L1S5 |
| C0006142 | Malignant neoplasm of breast | CHST9 | 83539 | carbohydrate sulfotransferase 9 | Q7L1S5 |
| C0027651 | Neoplasms | CHST9 | 83539 | carbohydrate sulfotransferase 9 | Q7L1S5 |
| C1306459 | Primary malignant neoplasm | B4GALNT4 | 338707 | beta-1,4-N-acetyl-galactosaminyltransferase 4 | Q76KP1 |
| C1140680 | Malignant neoplasm of ovary | B4GALNT4 | 338707 | beta-1,4-N-acetyl-galactosaminyltransferase 4 | Q76KP1 |
| C4014343 | MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42 | PGAP1 | 80055 | post-GPI attachment to proteins inositol deacylase 1 | Q75T13 |
| C0079541 | Holoprosencephaly | PGAP1 | 80055 | post-GPI attachment to proteins inositol deacylase 1 | Q75T13 |
| C0013421 | Dystonia | PGAP1 | 80055 | post-GPI attachment to proteins inositol deacylase 1 | Q75T13 |
| C0085584 | Encephalopathies | PGAP1 | 80055 | post-GPI attachment to proteins inositol deacylase 1 | Q75T13 |
| C0008489 | Chorea | PGAP1 | 80055 | post-GPI attachment to proteins inositol deacylase 1 | Q75T13 |
| C0036857 | Severe intellectual disability | PGAP1 | 80055 | post-GPI attachment to proteins inositol deacylase 1 | Q75T13 |
| C3714756 | Intellectual Disability | PGAP1 | 80055 | post-GPI attachment to proteins inositol deacylase 1 | Q75T13 |
| C0025958 | Microcephaly | PGAP1 | 80055 | post-GPI attachment to proteins inositol deacylase 1 | Q75T13 |
| C0234533 | Generalized seizures | PGAP1 | 80055 | post-GPI attachment to proteins inositol deacylase 1 | Q75T13 |
| C1292769 | Precursor B-cell lymphoblastic leukemia | PGAP1 | 80055 | post-GPI attachment to proteins inositol deacylase 1 | Q75T13 |
| C0520947 | Clumsiness - motor delay | PGAP1 | 80055 | post-GPI attachment to proteins inositol deacylase 1 | Q75T13 |
| C0013336 | Dwarfism | PGAP1 | 80055 | post-GPI attachment to proteins inositol deacylase 1 | Q75T13 |
| C0235946 | Cerebral atrophy | PGAP1 | 80055 | post-GPI attachment to proteins inositol deacylase 1 | Q75T13 |
| C0024790 | Paroxysmal nocturnal hemoglobinuria | PGAP1 | 80055 | post-GPI attachment to proteins inositol deacylase 1 | Q75T13 |
| C0015526 | Factor XII Deficiency | PGAP1 | 80055 | post-GPI attachment to proteins inositol deacylase 1 | Q75T13 |
| C1527366 | Salaam Seizures | PGAP1 | 80055 | post-GPI attachment to proteins inositol deacylase 1 | Q75T13 |
