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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 |
|---|---|---|---|---|---|
| C1319315 | Adenocarcinoma of large intestine | CLEC3A | 10143 | C-type lectin domain family 3 member A | O75596 |
| C2675481 | COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 | CLEC3A | 10143 | C-type lectin domain family 3 member A | O75596 |
| C3554460 | COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 | CLEC3A | 10143 | C-type lectin domain family 3 member A | O75596 |
| C0007102 | Malignant tumor of colon | CLEC3A | 10143 | C-type lectin domain family 3 member A | O75596 |
| C0009402 | Colorectal Carcinoma | CLEC3A | 10143 | C-type lectin domain family 3 member A | O75596 |
| C0029408 | Degenerative polyarthritis | CLEC3A | 10143 | C-type lectin domain family 3 member A | O75596 |
| C0006142 | Malignant neoplasm of breast | CLEC3A | 10143 | C-type lectin domain family 3 member A | O75596 |
| C1306459 | Primary malignant neoplasm | CLEC3A | 10143 | C-type lectin domain family 3 member A | O75596 |
| C1837315 | COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 | CLEC3A | 10143 | C-type lectin domain family 3 member A | O75596 |
| C0345904 | Malignant neoplasm of liver | CLEC2B | 9976 | C-type lectin domain family 2 member B | Q92478 |
| C0027651 | Neoplasms | CLEC2B | 9976 | C-type lectin domain family 2 member B | Q92478 |
| 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 |
