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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 ▲ |
|---|---|---|---|---|---|
| C0524524 | Pseudoaphakia | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C1510586 | Autism Spectrum Disorders | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0235946 | Cerebral atrophy | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0003811 | Cardiac Arrhythmia | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0162871 | Aortic Aneurysm, Abdominal | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C1704272 | Benign Prostatic Hyperplasia | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0009402 | Colorectal Carcinoma | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0151744 | Myocardial Ischemia | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0036421 | Systemic Scleroderma | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0030567 | Parkinson Disease | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0014175 | Endometriosis | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0010068 | Coronary heart disease | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0598608 | Hyperhomocysteinemia | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0242379 | Malignant neoplasm of lung | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0032460 | Polycystic Ovary Syndrome | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0022661 | Kidney Failure, Chronic | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0015934 | Fetal Growth Retardation | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0002736 | Amyotrophic Lateral Sclerosis | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0678222 | Breast Carcinoma | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0031099 | Periodontitis | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0497327 | Dementia | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0025202 | melanoma | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0014544 | Epilepsy | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0948008 | Ischemic stroke | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
