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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 |
|---|---|---|---|---|---|
| C0006826 | Malignant Neoplasms | CLEC3A | 10143 | C-type lectin domain family 3 member A | O75596 |
| 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 |
| 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 |
| C0008373 | Cholesteatoma | CLEC12B | 387837 | C-type lectin domain family 12 member B | Q2HXU8 |
| C1306459 | Primary malignant neoplasm | CLEC12B | 387837 | C-type lectin domain family 12 member B | Q2HXU8 |
| C0023467 | Leukemia, Myelocytic, Acute | CLEC12A | 160364 | C-type lectin domain family 12 member A | Q5QGZ9 |
| C0023465 | Acute monocytic leukemia | CLEC12A | 160364 | C-type lectin domain family 12 member A | Q5QGZ9 |
| C0023473 | Myeloid Leukemia, Chronic | CLEC12A | 160364 | C-type lectin domain family 12 member A | Q5QGZ9 |
| C1332977 | Childhood Leukemia | CLEC12A | 160364 | C-type lectin domain family 12 member A | Q5QGZ9 |
| C0021053 | Immune System Diseases | CLEC12A | 160364 | C-type lectin domain family 12 member A | Q5QGZ9 |
