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 |
---|---|---|---|---|---|
C0017638 | Glioma | CLEC5A | 23601 | C-type lectin domain containing 5A | Q9NY25 |
C0032302 | Mycoplasma pneumonia | CLEC5A | 23601 | C-type lectin domain containing 5A | Q9NY25 |
C0003850 | Arteriosclerosis | CLEC5A | 23601 | C-type lectin domain containing 5A | Q9NY25 |
C0014057 | Japanese Encephalitis | CLEC5A | 23601 | C-type lectin domain containing 5A | Q9NY25 |
C0349543 | Brain Glioblastoma | CLEC5A | 23601 | C-type lectin domain containing 5A | Q9NY25 |
C0029408 | Degenerative polyarthritis | CLEC5A | 23601 | C-type lectin domain containing 5A | Q9NY25 |
C0023434 | Chronic Lymphocytic Leukemia | CLEC17A | 388512 | C-type lectin domain containing 17A | Q6ZS10 |
C0026769 | Multiple Sclerosis | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0004364 | Autoimmune Diseases | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0020538 | Hypertensive disease | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0008312 | Primary biliary cirrhosis | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0001403 | Addison Disease | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0011854 | Diabetes Mellitus, Insulin-Dependent | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C4049006 | Selective immunoglobulin A deficiency | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0011849 | Diabetes Mellitus | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0008313 | Cholangitis, Sclerosing | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0010346 | Crohn Disease | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0948008 | Ischemic stroke | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0027051 | Myocardial Infarction | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0524620 | Metabolic Syndrome X | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0023892 | Biliary cirrhosis | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0002171 | Alopecia Areata | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C2936664 | Acquired Hypogammaglobulinemia | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0162538 | Immunoglobulin A deficiency (disorder) | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
C0019829 | Hodgkin Disease | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
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Last updated: August 19, 2024