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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 |
|---|---|---|---|---|---|
| C0007131 | Non-Small Cell Lung Carcinoma | FBXO17 | 115290 | F-box protein 17 | Q96EF6 |
| C1306459 | Primary malignant neoplasm | FBXO17 | 115290 | F-box protein 17 | Q96EF6 |
| C0027651 | Neoplasms | FBXO17 | 115290 | F-box protein 17 | Q96EF6 |
| C0020456 | Hyperglycemia | FBXO2 | 26232 | F-box protein 2 | Q9UK22 |
| C0024623 | Malignant neoplasm of stomach | FBXO2 | 26232 | F-box protein 2 | Q9UK22 |
| C0030567 | Parkinson Disease | FBXO2 | 26232 | F-box protein 2 | Q9UK22 |
| C0003873 | Rheumatoid Arthritis | FBXO2 | 26232 | F-box protein 2 | Q9UK22 |
| C0699791 | Stomach Carcinoma | FBXO2 | 26232 | F-box protein 2 | Q9UK22 |
| C0002395 | Alzheimer's Disease | FBXO2 | 26232 | F-box protein 2 | Q9UK22 |
| C0032460 | Polycystic Ovary Syndrome | FBXO44 | 93611 | F-box protein 44 | Q9H4M3 |
| C1136382 | Sclerocystic Ovaries | FBXO44 | 93611 | F-box protein 44 | Q9H4M3 |
| C0033578 | Prostatic Neoplasms | FBXO44 | 93611 | F-box protein 44 | Q9H4M3 |
| C0376358 | Malignant neoplasm of prostate | FBXO44 | 93611 | F-box protein 44 | Q9H4M3 |
| C0033860 | Psoriasis | FAM20B | 9917 | FAM20B glycosaminoglycan xylosylkinase | O75063 |
| C0013720 | Ehlers-Danlos Syndrome | FAM20B | 9917 | FAM20B glycosaminoglycan xylosylkinase | O75063 |
| C0432242 | Desbuquois syndrome | FAM20B | 9917 | FAM20B glycosaminoglycan xylosylkinase | O75063 |
| C0011195 | Dejerine-Sottas Disease (disorder) | FIG4 | 9896 | FIG4 phosphoinositide 5-phosphatase | Q92562 |
| C0154682 | Lateral Sclerosis | FIG4 | 9896 | FIG4 phosphoinositide 5-phosphatase | Q92562 |
| C1970011 | CHARCOT-MARIE-TOOTH DISEASE, TYPE 4J | FIG4 | 9896 | FIG4 phosphoinositide 5-phosphatase | Q92562 |
| C0027888 | Hereditary Motor and Sensory Neuropathies | FIG4 | 9896 | FIG4 phosphoinositide 5-phosphatase | Q92562 |
| C1857663 | Yunis Varon syndrome | FIG4 | 9896 | FIG4 phosphoinositide 5-phosphatase | Q92562 |
| C0085078 | Lysosomal Storage Diseases | FIG4 | 9896 | FIG4 phosphoinositide 5-phosphatase | Q92562 |
| C3711370 | Spastic Paraplegia Type 7 | FIG4 | 9896 | FIG4 phosphoinositide 5-phosphatase | Q92562 |
| C2675491 | AMYOTROPHIC LATERAL SCLEROSIS 11 | FIG4 | 9896 | FIG4 phosphoinositide 5-phosphatase | Q92562 |
| C0007959 | Charcot-Marie-Tooth Disease | FIG4 | 9896 | FIG4 phosphoinositide 5-phosphatase | Q92562 |
