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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 |
|---|---|---|---|---|---|
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | MGAT4A | 11320 | alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase A | Q9UM21 |
| C1306459 | Primary malignant neoplasm | MGAT4B | 11282 | alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B | Q9UQ53 |
| C1269683 | Major Depressive Disorder | MGAT4B | 11282 | alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B | Q9UQ53 |
| C0006826 | Malignant Neoplasms | MGAT4B | 11282 | alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B | Q9UQ53 |
| C0235974 | Pancreatic carcinoma | A4GNT | 51146 | alpha-1,4-N-acetylglucosaminyltransferase | Q9UNA3 |
| C0346647 | Malignant neoplasm of pancreas | A4GNT | 51146 | alpha-1,4-N-acetylglucosaminyltransferase | Q9UNA3 |
| C0006826 | Malignant Neoplasms | A4GNT | 51146 | alpha-1,4-N-acetylglucosaminyltransferase | Q9UNA3 |
| C0030297 | Pancreatic Neoplasm | A4GNT | 51146 | alpha-1,4-N-acetylglucosaminyltransferase | Q9UNA3 |
| C0017152 | Gastritis | A4GNT | 51146 | alpha-1,4-N-acetylglucosaminyltransferase | Q9UNA3 |
| C0030920 | Peptic Ulcer | A4GNT | 51146 | alpha-1,4-N-acetylglucosaminyltransferase | Q9UNA3 |
| C0278701 | Gastric Adenocarcinoma | A4GNT | 51146 | alpha-1,4-N-acetylglucosaminyltransferase | Q9UNA3 |
| C1306459 | Primary malignant neoplasm | A4GNT | 51146 | alpha-1,4-N-acetylglucosaminyltransferase | Q9UNA3 |
| C0699791 | Stomach Carcinoma | A4GNT | 51146 | alpha-1,4-N-acetylglucosaminyltransferase | Q9UNA3 |
| C0024623 | Malignant neoplasm of stomach | A4GNT | 51146 | alpha-1,4-N-acetylglucosaminyltransferase | Q9UNA3 |
| C0001418 | Adenocarcinoma | A4GNT | 51146 | alpha-1,4-N-acetylglucosaminyltransferase | Q9UNA3 |
| C2931008 | Congenital disorder of glycosylation type 2A | MGAT2 | 4247 | alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase | Q10469 |
| C0025517 | Metabolic Diseases | MGAT2 | 4247 | alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase | Q10469 |
| C0036572 | Seizures | MGAT2 | 4247 | alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase | Q10469 |
| C0028754 | Obesity | MGAT2 | 4247 | alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase | Q10469 |
| C0282577 | Congenital Disorders of Glycosylation | MGAT2 | 4247 | alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase | Q10469 |
| C0018784 | Sensorineural Hearing Loss (disorder) | MGAT2 | 4247 | alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase | Q10469 |
| C0027651 | Neoplasms | MGAT2 | 4247 | alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase | Q10469 |
| C0016202 | Flatfoot | MGAT2 | 4247 | alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase | Q10469 |
| C0085207 | Gestational Diabetes | MGAT2 | 4247 | alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase | Q10469 |
| C0011847 | Diabetes | MGAT2 | 4247 | alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase | Q10469 |
