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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 ▼ |
|---|---|---|---|---|---|
| C0021053 | Immune System Diseases | CLEC12A | 160364 | C-type lectin domain family 12 member A | Q5QGZ9 |
| C0023418 | leukemia | CLEC12A | 160364 | C-type lectin domain family 12 member A | Q5QGZ9 |
| C0014070 | Encephalomyelitis | CLEC12A | 160364 | C-type lectin domain family 12 member A | Q5QGZ9 |
| C1306459 | Primary malignant neoplasm | CLEC12A | 160364 | C-type lectin domain family 12 member A | Q5QGZ9 |
| C0026946 | Mycoses | CLEC12A | 160364 | C-type lectin domain family 12 member A | Q5QGZ9 |
| C0026470 | Monoclonal Gammopathy of Undetermined Significance | CLEC12A | 160364 | C-type lectin domain family 12 member A | Q5QGZ9 |
| C3463824 | MYELODYSPLASTIC SYNDROME | CLEC12A | 160364 | C-type lectin domain family 12 member A | Q5QGZ9 |
| C0003873 | Rheumatoid Arthritis | CLEC12A | 160364 | C-type lectin domain family 12 member A | Q5QGZ9 |
| C0027651 | Neoplasms | CLEC12A | 160364 | C-type lectin domain family 12 member A | Q5QGZ9 |
| C0006826 | Malignant Neoplasms | CLEC12A | 160364 | C-type lectin domain family 12 member A | Q5QGZ9 |
| C1378511 | Undifferentiated leukemia | CLEC12A | 160364 | C-type lectin domain family 12 member A | Q5QGZ9 |
| C0003864 | Arthritis | CLEC12A | 160364 | C-type lectin domain family 12 member A | Q5QGZ9 |
| C0280141 | Acute Undifferentiated Leukemia | CLEC12A | 160364 | C-type lectin domain family 12 member A | Q5QGZ9 |
| C0026769 | Multiple Sclerosis | CLEC12A | 160364 | C-type lectin domain family 12 member A | Q5QGZ9 |
| C0023449 | Acute lymphocytic leukemia | CLEC12A | 160364 | C-type lectin domain family 12 member A | Q5QGZ9 |
| C0153014 | Non-arthropod borne lymphocytic choriomeningitis | CLEC12A | 160364 | C-type lectin domain family 12 member A | Q5QGZ9 |
| C0026764 | Multiple Myeloma | CLEC12A | 160364 | C-type lectin domain family 12 member A | Q5QGZ9 |
| C0023434 | Chronic Lymphocytic Leukemia | CLEC12A | 160364 | C-type lectin domain family 12 member A | Q5QGZ9 |
| C0024419 | Waldenstrom Macroglobulinemia | CLEC12A | 160364 | C-type lectin domain family 12 member A | Q5QGZ9 |
| 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 |
| C3809092 | ADAMS-OLIVER SYNDROME 4 | EOGT | 285203 | EGF domain specific O-linked N-acetylglucosamine transferase | Q5NDL2 |
| C0026010 | Microphthalmos | EOGT | 285203 | EGF domain specific O-linked N-acetylglucosamine transferase | Q5NDL2 |
| C4551482 | Adams-Oliver syndrome 1 | EOGT | 285203 | EGF domain specific O-linked N-acetylglucosamine transferase | Q5NDL2 |
