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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 |
|---|---|---|---|---|---|
| C0005684 | Malignant neoplasm of urinary bladder | CDH13 | 1012 | cadherin 13 | P55290 |
| C0009324 | Ulcerative Colitis | CDH13 | 1012 | cadherin 13 | P55290 |
| C3642345 | Luminal A Breast Carcinoma | CDH13 | 1012 | cadherin 13 | P55290 |
| C0007134 | Renal Cell Carcinoma | CDH13 | 1012 | cadherin 13 | P55290 |
| C0027819 | Neuroblastoma | CDH13 | 1012 | cadherin 13 | P55290 |
| C0005586 | Bipolar Disorder | CDH13 | 1012 | cadherin 13 | P55290 |
| C0010346 | Crohn Disease | UST | 10090 | uronyl 2-sulfotransferase | Q9Y2C2 |
| C0038013 | Ankylosing spondylitis | UST | 10090 | uronyl 2-sulfotransferase | Q9Y2C2 |
| C0006826 | Malignant Neoplasms | UST | 10090 | uronyl 2-sulfotransferase | Q9Y2C2 |
| C0004238 | Atrial Fibrillation | UST | 10090 | uronyl 2-sulfotransferase | Q9Y2C2 |
| C0235480 | Paroxysmal atrial fibrillation | UST | 10090 | uronyl 2-sulfotransferase | Q9Y2C2 |
| C0269102 | Endometrioma | UST | 10090 | uronyl 2-sulfotransferase | Q9Y2C2 |
| C0029408 | Degenerative polyarthritis | UST | 10090 | uronyl 2-sulfotransferase | Q9Y2C2 |
| C0014175 | Endometriosis | UST | 10090 | uronyl 2-sulfotransferase | Q9Y2C2 |
| C0684249 | Carcinoma of lung | CYP3A7-CYP3A51P | 100861540 | CYP3A7-CYP3A51P readthrough | P24462 |
| C1306459 | Primary malignant neoplasm | CYP3A7-CYP3A51P | 100861540 | CYP3A7-CYP3A51P readthrough | P24462 |
| C1850318 | Omodysplasia type 1 | GPC6 | 10082 | glypican 6 | Q9Y625 |
| C0029456 | Osteoporosis | GPC6 | 10082 | glypican 6 | Q9Y625 |
| C0158266 | Intervertebral Disc Degeneration | GPC6 | 10082 | glypican 6 | Q9Y625 |
| C0019270 | Hernia | GPC6 | 10082 | glypican 6 | Q9Y625 |
| C0677886 | Epithelial ovarian cancer | GPC6 | 10082 | glypican 6 | Q9Y625 |
| C0036341 | Schizophrenia | GPC6 | 10082 | glypican 6 | Q9Y625 |
| C0005744 | Blepharophimosis | GPC6 | 10082 | glypican 6 | Q9Y625 |
| C2936816 | Micromelic dysplasia, congenital, with dislocation of radius | GPC6 | 10082 | glypican 6 | Q9Y625 |
| C3714756 | Intellectual Disability | GPC6 | 10082 | glypican 6 | Q9Y625 |
