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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 |
|---|---|---|---|---|---|
| C0011849 | Diabetes Mellitus | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C0024121 | Lung Neoplasms | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C0002395 | Alzheimer's Disease | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C0003873 | Rheumatoid Arthritis | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C0243026 | Sepsis | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C0034155 | Purpura, Thrombotic Thrombocytopenic | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C0038454 | Cerebrovascular accident | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C0005779 | Blood Coagulation Disorders | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C3714636 | Pneumonitis | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C1956346 | Coronary Artery Disease | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C0398650 | Immune thrombocytopenic purpura | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C2717961 | Thrombotic Microangiopathies | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C0032285 | Pneumonia | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C0040034 | Thrombocytopenia | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C0279702 | Conventional (Clear Cell) Renal Cell Carcinoma | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C0024623 | Malignant neoplasm of stomach | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C0025202 | melanoma | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C2931019 | Split hand foot deformity 1 | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C1861172 | Venous Thromboembolism | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C0010068 | Coronary heart disease | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C0242584 | Autoimmune thrombocytopenia | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C0035222 | Respiratory Distress Syndrome, Adult | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C0023467 | Leukemia, Myelocytic, Acute | CLEC12A | 160364 | C-type lectin domain family 12 member A | Q5QGZ9 |
| C0023465 | Acute monocytic leukemia | CLEC12A | 160364 | C-type lectin domain family 12 member A | Q5QGZ9 |
| C0023473 | Myeloid Leukemia, Chronic | CLEC12A | 160364 | C-type lectin domain family 12 member A | Q5QGZ9 |
