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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 ▲ |
|---|---|---|---|---|---|
| C0003873 | Rheumatoid Arthritis | B3GNT9 | 84752 | UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 9 | Q6UX72 |
| C2239176 | Liver carcinoma | CLEC4G | 339390 | C-type lectin domain family 4 member G | Q6UXB4 |
| C0282687 | Hemorrhagic Fever, Ebola | CLEC4G | 339390 | C-type lectin domain family 4 member G | Q6UXB4 |
| C4721806 | Carcinoma, Basal Cell | CLEC4G | 339390 | C-type lectin domain family 4 member G | Q6UXB4 |
| C0678222 | Breast Carcinoma | CLEC4G | 339390 | C-type lectin domain family 4 member G | Q6UXB4 |
| C0006142 | Malignant neoplasm of breast | CLEC4G | 339390 | C-type lectin domain family 4 member G | Q6UXB4 |
| 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 |
| C0004153 | Atherosclerosis | CLEC9A | 283420 | C-type lectin domain containing 9A | Q6UXN8 |
| C0042769 | Virus Diseases | CLEC9A | 283420 | C-type lectin domain containing 9A | Q6UXN8 |
| C0027651 | Neoplasms | CLEC9A | 283420 | C-type lectin domain containing 9A | Q6UXN8 |
| C3714636 | Pneumonitis | CLEC9A | 283420 | C-type lectin domain containing 9A | Q6UXN8 |
| 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 |
| C0699790 | Colon Carcinoma | CYP2R1 | 120227 | cytochrome P450 family 2 subfamily R member 1 | Q6VVX0 |
