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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 |
|---|---|---|---|---|---|
| C1691228 | Cystic Kidney Diseases | ALG8 | 79053 | ALG8 alpha-1,3-glucosyltransferase | Q9BVK2 |
| C0024236 | Lymphedema | ALG8 | 79053 | ALG8 alpha-1,3-glucosyltransferase | Q9BVK2 |
| C0011581 | Depressive disorder | ALG8 | 79053 | ALG8 alpha-1,3-glucosyltransferase | Q9BVK2 |
| C0009081 | Congenital clubfoot | ALG8 | 79053 | ALG8 alpha-1,3-glucosyltransferase | Q9BVK2 |
| C0018816 | Heart Septal Defects | ALG8 | 79053 | ALG8 alpha-1,3-glucosyltransferase | Q9BVK2 |
| C0086543 | Cataract | ALG8 | 79053 | ALG8 alpha-1,3-glucosyltransferase | Q9BVK2 |
| C2930997 | Congenital disorder of glycosylation type 1C | ALG6 | 29929 | ALG6 alpha-1,3-glucosyltransferase | Q9Y672 |
| C0282577 | Congenital Disorders of Glycosylation | ALG6 | 29929 | ALG6 alpha-1,3-glucosyltransferase | Q9Y672 |
| C0349653 | Congenital disorder of glycosylation type 1A | ALG6 | 29929 | ALG6 alpha-1,3-glucosyltransferase | Q9Y672 |
| C0038379 | Strabismus | ALG6 | 29929 | ALG6 alpha-1,3-glucosyltransferase | Q9Y672 |
| C0014544 | Epilepsy | ALG6 | 29929 | ALG6 alpha-1,3-glucosyltransferase | Q9Y672 |
| C0036572 | Seizures | ALG6 | 29929 | ALG6 alpha-1,3-glucosyltransferase | Q9Y672 |
| C0272375 | Antithrombin III Deficiency | ALG6 | 29929 | ALG6 alpha-1,3-glucosyltransferase | Q9Y672 |
| C0011991 | Diarrhea | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C0266551 | Congenital coloboma of iris | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C0279626 | Squamous cell carcinoma of esophagus | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C1832736 | CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Id | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C0235946 | Cerebral atrophy | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C0006826 | Malignant Neoplasms | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C0282577 | Congenital Disorders of Glycosylation | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C0006142 | Malignant neoplasm of breast | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C0023467 | Leukemia, Myelocytic, Acute | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C0038379 | Strabismus | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C0678222 | Breast Carcinoma | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
| C0554101 | Villous atrophy | ALG3 | 10195 | ALG3 alpha-1,3- mannosyltransferase | Q92685 |
