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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 |
|---|---|---|---|---|---|
| C0018621 | Hay fever | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C3495559 | Juvenile arthritis | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0152268 | Nodular Sclerosis Classical Hodgkin Lymphoma | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0205734 | Diabetes, Autoimmune | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0011847 | Diabetes | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0004943 | Behcet Syndrome | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C2607914 | Allergic rhinitis (disorder) | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0011615 | Dermatitis, Atopic | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0271650 | Impaired glucose tolerance | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0013595 | Eczema | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| 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 |
| C0796012 | Krause-Kivlin syndrome | POFUT2 | 23275 | protein O-fucosyltransferase 2 | Q9Y2G5 |
| C0036341 | Schizophrenia | POFUT2 | 23275 | protein O-fucosyltransferase 2 | Q9Y2G5 |
| C0024530 | Malaria | POFUT2 | 23275 | protein O-fucosyltransferase 2 | Q9Y2G5 |
| C0282577 | Congenital Disorders of Glycosylation | POFUT2 | 23275 | protein O-fucosyltransferase 2 | Q9Y2G5 |
