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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 |
|---|---|---|---|---|---|
| C0024266 | Lymphocytic Choriomeningitis | CLEC12A | 160364 | C-type lectin domain family 12 member A | Q5QGZ9 |
| C0010346 | Crohn Disease | CLEC12A | 160364 | C-type lectin domain family 12 member A | Q5QGZ9 |
| C1961102 | Precursor Cell Lymphoblastic Leukemia Lymphoma | CLEC12A | 160364 | C-type lectin domain family 12 member A | Q5QGZ9 |
| C0018784 | Sensorineural Hearing Loss (disorder) | TMTC2 | 160335 | transmembrane O-mannosyltransferase targeting cadherins 2 | Q8N394 |
| C0152136 | Low Tension Glaucoma | TMTC2 | 160335 | transmembrane O-mannosyltransferase targeting cadherins 2 | Q8N394 |
| C0017601 | Glaucoma | TMTC2 | 160335 | transmembrane O-mannosyltransferase targeting cadherins 2 | Q8N394 |
| C0013595 | Eczema | TMTC2 | 160335 | transmembrane O-mannosyltransferase targeting cadherins 2 | Q8N394 |
| C0004096 | Asthma | TMTC2 | 160335 | transmembrane O-mannosyltransferase targeting cadherins 2 | Q8N394 |
| C4082305 | Deaf Mutism | TMTC2 | 160335 | transmembrane O-mannosyltransferase targeting cadherins 2 | Q8N394 |
| C0339573 | Glaucoma, Primary Open Angle | TMTC2 | 160335 | transmembrane O-mannosyltransferase targeting cadherins 2 | Q8N394 |
| C0011053 | Deafness | TMTC2 | 160335 | transmembrane O-mannosyltransferase targeting cadherins 2 | Q8N394 |
| C0004096 | Asthma | DAD1 | 1603 | defender against cell death 1 | P61803 |
| C0206754 | Neuroendocrine Tumors | DAD1 | 1603 | defender against cell death 1 | P61803 |
| C0264408 | Childhood asthma | DAD1 | 1603 | defender against cell death 1 | P61803 |
| C0149925 | Small cell carcinoma of lung | DAD1 | 1603 | defender against cell death 1 | P61803 |
| C1306459 | Primary malignant neoplasm | DAD1 | 1603 | defender against cell death 1 | P61803 |
| C0004763 | Barrett Esophagus | DAD1 | 1603 | defender against cell death 1 | P61803 |
| C0155877 | Allergic asthma | DAD1 | 1603 | defender against cell death 1 | P61803 |
| C0006826 | Malignant Neoplasms | DAD1 | 1603 | defender against cell death 1 | P61803 |
| C0026946 | Mycoses | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C0041234 | Chagas Disease | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C0085436 | Meningitis, Cryptococcal | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C0006826 | Malignant Neoplasms | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C0009186 | Coccidioidomycosis | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C0041296 | Tuberculosis | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
