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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 |
|---|---|---|---|---|---|
| C0007570 | Celiac Disease | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0264408 | Childhood asthma | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0524851 | Neurodegenerative Disorders | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C1561643 | Chronic Kidney Diseases | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0009447 | Common Variable Immunodeficiency | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0242380 | Libman-Sacks Disease | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0038013 | Ankylosing spondylitis | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C1285162 | Degenerative disorder | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0042170 | Uveomeningoencephalitic Syndrome | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0009324 | Ulcerative Colitis | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0341106 | Eosinophilic esophagitis | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0023434 | Chronic Lymphocytic Leukemia | CLEC17A | 388512 | C-type lectin domain containing 17A | Q6ZS10 |
| C1836230 | HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO | CLEC18B | 497190 | C-type lectin domain family 18 member B | Q6UXF7 |
| C1621958 | Glioblastoma Multiforme | CLEC18B | 497190 | C-type lectin domain family 18 member B | Q6UXF7 |
| C0006826 | Malignant Neoplasms | CLEC18B | 497190 | C-type lectin domain family 18 member B | Q6UXF7 |
| C0017636 | Glioblastoma | CLEC18B | 497190 | C-type lectin domain family 18 member B | Q6UXF7 |
| C0278878 | Adult Glioblastoma | CLEC18B | 497190 | C-type lectin domain family 18 member B | Q6UXF7 |
| C1306459 | Primary malignant neoplasm | CLEC18B | 497190 | C-type lectin domain family 18 member B | Q6UXF7 |
| C0004030 | Aspergillosis | CLEC1A | 51267 | C-type lectin domain family 1 member A | Q8NC01 |
| C0006826 | Malignant Neoplasms | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C0042769 | Virus Diseases | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C0000768 | Congenital Abnormality | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C0027651 | Neoplasms | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C0699791 | Stomach Carcinoma | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C0014116 | Endocardial Cushion Defects | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
