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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 |
|---|---|---|---|---|---|
| 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 |
| 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 |
| C4317295 | Congenital disorder of glycosylation type 1s | ALG8 | 79053 | ALG8 alpha-1,3-glucosyltransferase | Q9BVK2 |
| C0011991 | Diarrhea | ALG8 | 79053 | ALG8 alpha-1,3-glucosyltransferase | Q9BVK2 |
| C0015934 | Fetal Growth Retardation | ALG8 | 79053 | ALG8 alpha-1,3-glucosyltransferase | Q9BVK2 |
| C2931002 | Congenital disorder of glycosylation type 1H | ALG8 | 79053 | ALG8 alpha-1,3-glucosyltransferase | Q9BVK2 |
| C0282577 | Congenital Disorders of Glycosylation | ALG8 | 79053 | ALG8 alpha-1,3-glucosyltransferase | Q9BVK2 |
| C0010417 | Cryptorchidism | ALG8 | 79053 | ALG8 alpha-1,3-glucosyltransferase | Q9BVK2 |
| C0079924 | Oligohydramnios | ALG8 | 79053 | ALG8 alpha-1,3-glucosyltransferase | Q9BVK2 |
| C0015930 | Fetal Distress | ALG8 | 79053 | ALG8 alpha-1,3-glucosyltransferase | Q9BVK2 |
| C0020224 | Polyhydramnios | ALG8 | 79053 | ALG8 alpha-1,3-glucosyltransferase | Q9BVK2 |
| C0020676 | Hypothyroidism | ALG8 | 79053 | ALG8 alpha-1,3-glucosyltransferase | Q9BVK2 |
| C3887499 | Renal cyst | ALG8 | 79053 | ALG8 alpha-1,3-glucosyltransferase | Q9BVK2 |
| C0040034 | Thrombocytopenia | ALG8 | 79053 | ALG8 alpha-1,3-glucosyltransferase | Q9BVK2 |
| C0158683 | Polycystic liver disease | ALG8 | 79053 | ALG8 alpha-1,3-glucosyltransferase | Q9BVK2 |
