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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 ▲ |
|---|---|---|---|---|---|
| C0270962 | Multi-core congenital myopathy | POMT1 | 10585 | protein O-mannosyltransferase 1 | Q9Y6A1 |
| C0338502 | Hypoplasia of the optic nerve | POMT1 | 10585 | protein O-mannosyltransferase 1 | Q9Y6A1 |
| C0026010 | Microphthalmos | POMT1 | 10585 | protein O-mannosyltransferase 1 | Q9Y6A1 |
| C3809221 | MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 14 | POMT1 | 10585 | protein O-mannosyltransferase 1 | Q9Y6A1 |
| C0270790 | Quadriparesis | POMT1 | 10585 | protein O-mannosyltransferase 1 | Q9Y6A1 |
| C0266544 | Microcornea | POMT1 | 10585 | protein O-mannosyltransferase 1 | Q9Y6A1 |
| C0008925 | Cleft Palate | POMT1 | 10585 | protein O-mannosyltransferase 1 | Q9Y6A1 |
| C0231528 | Myalgia | POMT1 | 10585 | protein O-mannosyltransferase 1 | Q9Y6A1 |
| C0029124 | Optic Atrophy | POMT1 | 10585 | protein O-mannosyltransferase 1 | Q9Y6A1 |
| C1869123 | Limb-girdle muscular dystrophy type 2A | POMT1 | 10585 | protein O-mannosyltransferase 1 | Q9Y6A1 |
| C0015393 | Eye Abnormalities | POMT1 | 10585 | protein O-mannosyltransferase 1 | Q9Y6A1 |
| C0010038 | Corneal Opacity | POMT1 | 10585 | protein O-mannosyltransferase 1 | Q9Y6A1 |
| C0344530 | Congenital keratoglobus | POMT1 | 10585 | protein O-mannosyltransferase 1 | Q9Y6A1 |
| C0575158 | Kyphoscoliosis deformity of spine | POMT1 | 10585 | protein O-mannosyltransferase 1 | Q9Y6A1 |
| C0456909 | Blindness | POMT1 | 10585 | protein O-mannosyltransferase 1 | Q9Y6A1 |
| C0010964 | Dandy-Walker Syndrome | POMT1 | 10585 | protein O-mannosyltransferase 1 | Q9Y6A1 |
| C0008924 | Cleft upper lip | POMT1 | 10585 | protein O-mannosyltransferase 1 | Q9Y6A1 |
| C0035305 | Retinal Detachment | POMT1 | 10585 | protein O-mannosyltransferase 1 | Q9Y6A1 |
| C4015184 | MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 12 | POMT1 | 10585 | protein O-mannosyltransferase 1 | Q9Y6A1 |
| C0009363 | Congenital ocular coloboma (disorder) | POMT1 | 10585 | protein O-mannosyltransferase 1 | Q9Y6A1 |
| C0026848 | Myopathy | POMT1 | 10585 | protein O-mannosyltransferase 1 | Q9Y6A1 |
| C0015469 | Facial paralysis | POMT1 | 10585 | protein O-mannosyltransferase 1 | Q9Y6A1 |
| C0079541 | Holoprosencephaly | POMT1 | 10585 | protein O-mannosyltransferase 1 | Q9Y6A1 |
| C1384666 | hearing impairment | POMT1 | 10585 | protein O-mannosyltransferase 1 | Q9Y6A1 |
| C1879312 | Agyria | POMT1 | 10585 | protein O-mannosyltransferase 1 | Q9Y6A1 |
