Table Filtering
Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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 |
| C0038454 | Cerebrovascular accident | MAN2B2 | 23324 | mannosidase alpha class 2B member 2 | Q9Y2E5 |
| C0021051 | Immunologic Deficiency Syndromes | MAN2B2 | 23324 | mannosidase alpha class 2B member 2 | Q9Y2E5 |
| C0152018 | Esophageal carcinoma | MAN2C1 | 4123 | mannosidase alpha class 2C member 1 | Q9NTJ4 |
| C0024748 | alpha-Mannosidosis | MAN2C1 | 4123 | mannosidase alpha class 2C member 1 | Q9NTJ4 |
| C0006142 | Malignant neoplasm of breast | MAN2C1 | 4123 | mannosidase alpha class 2C member 1 | Q9NTJ4 |
| C3714756 | Intellectual Disability | MAN2C1 | 4123 | mannosidase alpha class 2C member 1 | Q9NTJ4 |
| C1458155 | Mammary Neoplasms | MAN2C1 | 4123 | mannosidase alpha class 2C member 1 | Q9NTJ4 |
