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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 |
|---|---|---|---|---|---|
| C0001418 | Adenocarcinoma | NAMPT | 10135 | nicotinamide phosphoribosyltransferase | P43490 |
| C0699791 | Stomach Carcinoma | NAMPT | 10135 | nicotinamide phosphoribosyltransferase | P43490 |
| C0042373 | Vascular Diseases | NAMPT | 10135 | nicotinamide phosphoribosyltransferase | P43490 |
| C0013274 | Patent ductus arteriosus | NAMPT | 10135 | nicotinamide phosphoribosyltransferase | P43490 |
| C0006826 | Malignant Neoplasms | CLEC3A | 10143 | C-type lectin domain family 3 member A | O75596 |
| C1319315 | Adenocarcinoma of large intestine | CLEC3A | 10143 | C-type lectin domain family 3 member A | O75596 |
| C2675481 | COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 | CLEC3A | 10143 | C-type lectin domain family 3 member A | O75596 |
| C3554460 | COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 | CLEC3A | 10143 | C-type lectin domain family 3 member A | O75596 |
| C0007102 | Malignant tumor of colon | CLEC3A | 10143 | C-type lectin domain family 3 member A | O75596 |
| C0009402 | Colorectal Carcinoma | CLEC3A | 10143 | C-type lectin domain family 3 member A | O75596 |
| C0029408 | Degenerative polyarthritis | CLEC3A | 10143 | C-type lectin domain family 3 member A | O75596 |
| C0006142 | Malignant neoplasm of breast | CLEC3A | 10143 | C-type lectin domain family 3 member A | O75596 |
| C1306459 | Primary malignant neoplasm | CLEC3A | 10143 | C-type lectin domain family 3 member A | O75596 |
| C1837315 | COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 | CLEC3A | 10143 | C-type lectin domain family 3 member A | O75596 |
| C0242379 | Malignant neoplasm of lung | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C0006826 | Malignant Neoplasms | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C0020538 | Hypertensive disease | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C0022658 | Kidney Diseases | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C0028754 | Obesity | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C0013371 | Shigella Infections | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C0278878 | Adult Glioblastoma | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C0007222 | Cardiovascular Diseases | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C0011849 | Diabetes Mellitus | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C0028756 | Obesity, Morbid | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C1861303 | SYNOVITIS, GRANULOMATOUS, WITH UVEITIS AND CRANIAL NEUROPATHIES (disorder) | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
