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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 |
|---|---|---|---|---|---|
| C0029463 | Osteosarcoma | INPP4B | 8821 | inositol polyphosphate-4-phosphatase type II B | O15327 |
| C0278601 | Inflammatory Breast Carcinoma | INPP4B | 8821 | inositol polyphosphate-4-phosphatase type II B | O15327 |
| C0242379 | Malignant neoplasm of lung | INPP4B | 8821 | inositol polyphosphate-4-phosphatase type II B | O15327 |
| C1842675 | AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder) | INPP4B | 8821 | inositol polyphosphate-4-phosphatase type II B | O15327 |
| C0029456 | Osteoporosis | INPP4B | 8821 | inositol polyphosphate-4-phosphatase type II B | O15327 |
| C0585442 | Osteosarcoma of bone | INPP4B | 8821 | inositol polyphosphate-4-phosphatase type II B | O15327 |
| C1879321 | Acute Myeloid Leukemia (AML-M2) | INPP4B | 8821 | inositol polyphosphate-4-phosphatase type II B | O15327 |
| C1306837 | Papillary Renal Cell Carcinoma | INPP4B | 8821 | inositol polyphosphate-4-phosphatase type II B | O15327 |
| C0007847 | Malignant tumor of cervix | INPP4B | 8821 | inositol polyphosphate-4-phosphatase type II B | O15327 |
| C1332979 | Childhood Lymphoma | INPP4B | 8821 | inositol polyphosphate-4-phosphatase type II B | O15327 |
| C0007115 | Malignant neoplasm of thyroid | INPP4B | 8821 | inositol polyphosphate-4-phosphatase type II B | O15327 |
| C0302592 | Cervix carcinoma | INPP4B | 8821 | inositol polyphosphate-4-phosphatase type II B | O15327 |
| C3542025 | AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE | INPP4B | 8821 | inositol polyphosphate-4-phosphatase type II B | O15327 |
| C0023465 | Acute monocytic leukemia | INPP4B | 8821 | inositol polyphosphate-4-phosphatase type II B | O15327 |
| C1332206 | Adult Lymphoma | INPP4B | 8821 | inositol polyphosphate-4-phosphatase type II B | O15327 |
| C0014544 | Epilepsy | DPM2 | 8818 | dolichyl-phosphate mannosyltransferase subunit 2, regulatory | O94777 |
| C3554385 | CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iu | DPM2 | 8818 | dolichyl-phosphate mannosyltransferase subunit 2, regulatory | O94777 |
| C0241005 | Creatine phosphokinase serum increased | DPM2 | 8818 | dolichyl-phosphate mannosyltransferase subunit 2, regulatory | O94777 |
| C0026850 | Muscular Dystrophy | DPM2 | 8818 | dolichyl-phosphate mannosyltransferase subunit 2, regulatory | O94777 |
| C0017606 | Primary angle-closure glaucoma | DPM2 | 8818 | dolichyl-phosphate mannosyltransferase subunit 2, regulatory | O94777 |
| C0206368 | Exfoliation Syndrome | DPM2 | 8818 | dolichyl-phosphate mannosyltransferase subunit 2, regulatory | O94777 |
| C0020224 | Polyhydramnios | DPM2 | 8818 | dolichyl-phosphate mannosyltransferase subunit 2, regulatory | O94777 |
| C0272375 | Antithrombin III Deficiency | DPM2 | 8818 | dolichyl-phosphate mannosyltransferase subunit 2, regulatory | O94777 |
| C0036439 | Scoliosis, unspecified | DPM2 | 8818 | dolichyl-phosphate mannosyltransferase subunit 2, regulatory | O94777 |
| C0017601 | Glaucoma | DPM2 | 8818 | dolichyl-phosphate mannosyltransferase subunit 2, regulatory | O94777 |
