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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 ▲ |
|---|---|---|---|---|---|
| C0010054 | Coronary Arteriosclerosis | PIK3C2A | 5286 | phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha | O00443 |
| C0010417 | Cryptorchidism | PIK3C2A | 5286 | phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha | O00443 |
| C0040034 | Thrombocytopenia | PIK3C2A | 5286 | phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha | O00443 |
| C1384666 | hearing impairment | PIK3C2A | 5286 | phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha | O00443 |
| C0238198 | Gastrointestinal Stromal Tumors | PIK3C2A | 5286 | phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha | O00443 |
| C1836230 | HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO | PIK3C2A | 5286 | phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha | O00443 |
| C0010068 | Coronary heart disease | PIK3C2A | 5286 | phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha | O00443 |
| C0036220 | Kaposi Sarcoma | PIK3C2A | 5286 | phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha | O00443 |
| C0023470 | Myeloid Leukemia | PIK3C2A | 5286 | phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha | O00443 |
| C4082304 | Oligodontia | PIK3C2A | 5286 | phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha | O00443 |
| C0678222 | Breast Carcinoma | PIK3C2A | 5286 | phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha | O00443 |
| C0027651 | Neoplasms | PIK3C2A | 5286 | phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha | O00443 |
| C0338451 | Frontotemporal dementia | GFRA2 | 2675 | GDNF family receptor alpha 2 | O00451 |
| C0001430 | Adenoma | GFRA2 | 2675 | GDNF family receptor alpha 2 | O00451 |
| C0339543 | Epiretinal Membrane | GFRA2 | 2675 | GDNF family receptor alpha 2 | O00451 |
| C0019569 | Hirschsprung Disease | GFRA2 | 2675 | GDNF family receptor alpha 2 | O00451 |
| C0027651 | Neoplasms | GFRA2 | 2675 | GDNF family receptor alpha 2 | O00451 |
| C0442874 | Neuropathy | GFRA2 | 2675 | GDNF family receptor alpha 2 | O00451 |
| C0036341 | Schizophrenia | GFRA2 | 2675 | GDNF family receptor alpha 2 | O00451 |
| C0235974 | Pancreatic carcinoma | GFRA2 | 2675 | GDNF family receptor alpha 2 | O00451 |
| C0700095 | Central neuroblastoma | GFRA2 | 2675 | GDNF family receptor alpha 2 | O00451 |
| C0005586 | Bipolar Disorder | GFRA2 | 2675 | GDNF family receptor alpha 2 | O00451 |
| C0009402 | Colorectal Carcinoma | GFRA2 | 2675 | GDNF family receptor alpha 2 | O00451 |
| C0242422 | Parkinsonian Disorders | GFRA2 | 2675 | GDNF family receptor alpha 2 | O00451 |
| C0686347 | Tardive Dyskinesia | GFRA2 | 2675 | GDNF family receptor alpha 2 | O00451 |
