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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 ▼ |
|---|---|---|---|---|---|
| C0024748 | alpha-Mannosidosis | MAN2B1 | 4125 | mannosidase alpha class 2B member 1 | O00754 |
| C1257960 | Mannosidase Deficiency Diseases | MAN2B1 | 4125 | mannosidase alpha class 2B member 1 | O00754 |
| C0026650 | Movement Disorders | MAN2B1 | 4125 | mannosidase alpha class 2B member 1 | O00754 |
| C0019294 | Hernia, Inguinal | MAN2B1 | 4125 | mannosidase alpha class 2B member 1 | O00754 |
| C0038016 | Spondylolisthesis | MAN2B1 | 4125 | mannosidase alpha class 2B member 1 | O00754 |
| C0017921 | Glycogen storage disease type II | MAN2B1 | 4125 | mannosidase alpha class 2B member 1 | O00754 |
| C0085078 | Lysosomal Storage Diseases | MAN2B1 | 4125 | mannosidase alpha class 2B member 1 | O00754 |
| C0020555 | Hypertrichosis | MAN2B1 | 4125 | mannosidase alpha class 2B member 1 | O00754 |
| C0035304 | Retinal Degeneration | MAN2B1 | 4125 | mannosidase alpha class 2B member 1 | O00754 |
| C3714756 | Intellectual Disability | MAN2B1 | 4125 | mannosidase alpha class 2B member 1 | O00754 |
| C0017661 | IGA Glomerulonephritis | MAN2B1 | 4125 | mannosidase alpha class 2B member 1 | O00754 |
| C0376480 | Gingival Overgrowth | MAN2B1 | 4125 | mannosidase alpha class 2B member 1 | O00754 |
| C0235946 | Cerebral atrophy | MAN2B1 | 4125 | mannosidase alpha class 2B member 1 | O00754 |
| C1855114 | Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency | MAN2B1 | 4125 | mannosidase alpha class 2B member 1 | O00754 |
| C0028738 | Nystagmus | MAN2B1 | 4125 | mannosidase alpha class 2B member 1 | O00754 |
| C0242383 | Age related macular degeneration | MAN2B1 | 4125 | mannosidase alpha class 2B member 1 | O00754 |
| C0018784 | Sensorineural Hearing Loss (disorder) | MAN2B1 | 4125 | mannosidase alpha class 2B member 1 | O00754 |
| C0086795 | Pfaundler-Hurler Syndrome | MAN2B1 | 4125 | mannosidase alpha class 2B member 1 | O00754 |
| C0027651 | Neoplasms | PIK3C2B | 5287 | phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 beta | O00750 |
| C0376358 | Malignant neoplasm of prostate | PIK3C2B | 5287 | phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 beta | O00750 |
| C0038454 | Cerebrovascular accident | PIK3C2B | 5287 | phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 beta | O00750 |
| C0751606 | Adult Acute Lymphocytic Leukemia | PIK3C2B | 5287 | phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 beta | O00750 |
| C0600139 | Prostate carcinoma | PIK3C2B | 5287 | phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 beta | O00750 |
| C0017638 | Glioma | PIK3C2B | 5287 | phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 beta | O00750 |
| C0036421 | Systemic Scleroderma | PIK3C2B | 5287 | phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 beta | O00750 |
