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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 |
|---|---|---|---|---|---|
| C0041296 | Tuberculosis | CLEC9A | 283420 | C-type lectin domain containing 9A | Q6UXN8 |
| C0001175 | Acquired Immunodeficiency Syndrome | CLEC9A | 283420 | C-type lectin domain containing 9A | Q6UXN8 |
| C0021400 | Influenza | CLEC9A | 283420 | C-type lectin domain containing 9A | Q6UXN8 |
| C0026918 | Mycobacterium Infections | CLEC9A | 283420 | C-type lectin domain containing 9A | Q6UXN8 |
| C0019348 | Herpes Simplex Infections | CLEC9A | 283420 | C-type lectin domain containing 9A | Q6UXN8 |
| C0003850 | Arteriosclerosis | CLEC9A | 283420 | C-type lectin domain containing 9A | Q6UXN8 |
| C0021051 | Immunologic Deficiency Syndromes | CLEC9A | 283420 | C-type lectin domain containing 9A | Q6UXN8 |
| C0032285 | Pneumonia | CLEC9A | 283420 | C-type lectin domain containing 9A | Q6UXN8 |
| 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 |
| C0019061 | Hemolytic-Uremic Syndrome | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C0272286 | Thrombocytopenia due to platelet alloimmunization | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C0039585 | Androgen-Insensitivity Syndrome | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C2239176 | Liver carcinoma | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C1306459 | Primary malignant neoplasm | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C0010054 | Coronary Arteriosclerosis | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C0023895 | Liver diseases | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C0011847 | Diabetes | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C0948008 | Ischemic stroke | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
| C0018939 | Hematological Disease | CLEC1B | 51266 | C-type lectin domain family 1 member B | Q9P126 |
