Table Filtering
Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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 |
|---|---|---|---|---|---|
| C0278878 | Adult Glioblastoma | ALG2 | 85365 | ALG2 alpha-1,3/1,6-mannosyltransferase | Q9H553 |
| C3714756 | Intellectual Disability | ALG2 | 85365 | ALG2 alpha-1,3/1,6-mannosyltransferase | Q9H553 |
| C0036439 | Scoliosis, unspecified | ALG2 | 85365 | ALG2 alpha-1,3/1,6-mannosyltransferase | Q9H553 |
| C0036572 | Seizures | ALG2 | 85365 | ALG2 alpha-1,3/1,6-mannosyltransferase | Q9H553 |
| C0017636 | Glioblastoma | ALG2 | 85365 | ALG2 alpha-1,3/1,6-mannosyltransferase | Q9H553 |
| 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 |
| 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 |
