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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 |
|---|---|---|---|---|---|
| C0476089 | Endometrial Carcinoma | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C1845543 | Mental Retardation, X-Linked, with Epilepsy | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C0151773 | Bone marrow depression | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C0025945 | Microangiopathy, Diabetic | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C0007192 | Cardiomyopathy, Alcoholic | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C0009402 | Colorectal Carcinoma | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C0006142 | Malignant neoplasm of breast | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C0003504 | Aortic Valve Insufficiency | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C0030567 | Parkinson Disease | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C0017921 | Glycogen storage disease type II | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C0007820 | Cerebrovascular Disorders | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C0687720 | Central Diabetes Insipidus | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C0007103 | Malignant neoplasm of endometrium | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C0035078 | Kidney Failure | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C0027651 | Neoplasms | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C0520947 | Clumsiness - motor delay | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C0376358 | Malignant neoplasm of prostate | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C0016202 | Flatfoot | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C1561643 | Chronic Kidney Diseases | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C0013537 | Eclampsia | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C0678222 | Breast Carcinoma | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C1136249 | Mental Retardation, X-Linked | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C1563705 | Nephrogenic Diabetes Insipidus, Type I | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
| C0018213 | Graves Disease | ATP6AP2 | 10159 | ATPase H+ transporting accessory protein 2 | O75787 |
