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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 |
|---|---|---|---|---|---|
| C4317295 | Congenital disorder of glycosylation type 1s | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C1306459 | Primary malignant neoplasm | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C1168401 | Squamous cell carcinoma of the head and neck | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C0027651 | Neoplasms | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C3279947 | NAIL DISORDER, NONSYNDROMIC CONGENITAL, 9 | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C0036572 | Seizures | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C0029124 | Optic Atrophy | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C0684276 | Hypsarrhythmia | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C0025958 | Microcephaly | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C0009081 | Congenital clubfoot | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C0276496 | Familial Alzheimer Disease (FAD) | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C0280324 | Laryngeal Squamous Cell Carcinoma | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C1836669 | CONGENITAL DISORDER OF GLYCOSYLATION, TYPE If | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C4015597 | MYASTHENIC SYNDROME, CONGENITAL, 14 | ALG2 | 85365 | ALG2 alpha-1,3/1,6-mannosyltransferase | Q9H553 |
| C0009363 | Congenital ocular coloboma (disorder) | ALG2 | 85365 | ALG2 alpha-1,3/1,6-mannosyltransferase | Q9H553 |
| C3665347 | Visual Impairment | ALG2 | 85365 | ALG2 alpha-1,3/1,6-mannosyltransferase | Q9H553 |
| C0027651 | Neoplasms | ALG2 | 85365 | ALG2 alpha-1,3/1,6-mannosyltransferase | Q9H553 |
| C0751882 | Myasthenic Syndromes, Congenital | ALG2 | 85365 | ALG2 alpha-1,3/1,6-mannosyltransferase | Q9H553 |
| C0684276 | Hypsarrhythmia | ALG2 | 85365 | ALG2 alpha-1,3/1,6-mannosyltransferase | Q9H553 |
| C1306459 | Primary malignant neoplasm | ALG2 | 85365 | ALG2 alpha-1,3/1,6-mannosyltransferase | Q9H553 |
| C0026848 | Myopathy | ALG2 | 85365 | ALG2 alpha-1,3/1,6-mannosyltransferase | Q9H553 |
| C0266551 | Congenital coloboma of iris | ALG2 | 85365 | ALG2 alpha-1,3/1,6-mannosyltransferase | Q9H553 |
| C0241005 | Creatine phosphokinase serum increased | ALG2 | 85365 | ALG2 alpha-1,3/1,6-mannosyltransferase | Q9H553 |
| C0751883 | Congenital Myasthenic Syndromes, Postsynaptic | ALG2 | 85365 | ALG2 alpha-1,3/1,6-mannosyltransferase | Q9H553 |
| C0282577 | Congenital Disorders of Glycosylation | ALG2 | 85365 | ALG2 alpha-1,3/1,6-mannosyltransferase | Q9H553 |
