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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 |
|---|---|---|---|---|---|
| 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 |
| C0279639 | Mucinous adenocarcinoma of colon | CHST4 | 10164 | carbohydrate sulfotransferase 4 | Q8NCG5 |
| C0027651 | Neoplasms | CHST4 | 10164 | carbohydrate sulfotransferase 4 | Q8NCG5 |
| C0009319 | Colitis | CHST4 | 10164 | carbohydrate sulfotransferase 4 | Q8NCG5 |
| C0029408 | Degenerative polyarthritis | CHST4 | 10164 | carbohydrate sulfotransferase 4 | Q8NCG5 |
| C0699790 | Colon Carcinoma | CHST4 | 10164 | carbohydrate sulfotransferase 4 | Q8NCG5 |
| C0007102 | Malignant tumor of colon | CHST4 | 10164 | carbohydrate sulfotransferase 4 | Q8NCG5 |
| C1956346 | Coronary Artery Disease | LPCAT3 | 10162 | lysophosphatidylcholine acyltransferase 3 | Q6P1A2 |
| C0010068 | Coronary heart disease | LPCAT3 | 10162 | lysophosphatidylcholine acyltransferase 3 | Q6P1A2 |
| C0002875 | Cooley's anemia | LPCAT3 | 10162 | lysophosphatidylcholine acyltransferase 3 | Q6P1A2 |
| C0010054 | Coronary Arteriosclerosis | LPCAT3 | 10162 | lysophosphatidylcholine acyltransferase 3 | Q6P1A2 |
| C0003850 | Arteriosclerosis | LPCAT3 | 10162 | lysophosphatidylcholine acyltransferase 3 | Q6P1A2 |
| C0020456 | Hyperglycemia | LPCAT3 | 10162 | lysophosphatidylcholine acyltransferase 3 | Q6P1A2 |
| C0004153 | Atherosclerosis | LPCAT3 | 10162 | lysophosphatidylcholine acyltransferase 3 | Q6P1A2 |
| C0085580 | Essential Hypertension | LPCAT3 | 10162 | lysophosphatidylcholine acyltransferase 3 | Q6P1A2 |
| C0027651 | Neoplasms | LPCAT3 | 10162 | lysophosphatidylcholine acyltransferase 3 | Q6P1A2 |
| C0042373 | Vascular Diseases | LPCAT3 | 10162 | lysophosphatidylcholine acyltransferase 3 | Q6P1A2 |
| C0002895 | Anemia, Sickle Cell | LPCAT3 | 10162 | lysophosphatidylcholine acyltransferase 3 | Q6P1A2 |
