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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 |
| C0376358 | Malignant neoplasm of prostate | CLGN | 1047 | calmegin | O14967 |
| C0036631 | Seminoma | CLGN | 1047 | calmegin | O14967 |
| C0600139 | Prostate carcinoma | CLGN | 1047 | calmegin | O14967 |
| C0678222 | Breast Carcinoma | CLGN | 1047 | calmegin | O14967 |
| C0006142 | Malignant neoplasm of breast | CLGN | 1047 | calmegin | O14967 |
| C0027877 | Neuronal Ceroid-Lipofuscinoses | CLN5 | 1203 | CLN5 intracellular trafficking protein | O75503 |
| C0751783 | Lafora Disease | CLN5 | 1203 | CLN5 intracellular trafficking protein | O75503 |
| C1850442 | CEROID LIPOFUSCINOSIS, NEURONAL, 5 | CLN5 | 1203 | CLN5 intracellular trafficking protein | O75503 |
| C1838571 | Ceroid Lipofuscinosis, Neuronal, 7 | CLN5 | 1203 | CLN5 intracellular trafficking protein | O75503 |
| C0235946 | Cerebral atrophy | CLN5 | 1203 | CLN5 intracellular trafficking protein | O75503 |
| C0022340 | Late-Infantile Neuronal Ceroid Lipfuscinosis | CLN5 | 1203 | CLN5 intracellular trafficking protein | O75503 |
| C1864923 | Northern epilepsy syndrome | CLN5 | 1203 | CLN5 intracellular trafficking protein | O75503 |
| C0751383 | Juvenile Neuronal Ceroid Lipofuscinosis | CLN5 | 1203 | CLN5 intracellular trafficking protein | O75503 |
| C1866282 | CEROID LIPOFUSCINOSIS, NEURONAL, 6 | CLN5 | 1203 | CLN5 intracellular trafficking protein | O75503 |
| C0162672 | MERRF Syndrome | CLN5 | 1203 | CLN5 intracellular trafficking protein | O75503 |
| C1838570 | CEROID LIPOFUSCINOSIS, NEURONAL, 8 | CLN5 | 1203 | CLN5 intracellular trafficking protein | O75503 |
| C0233844 | Clumsiness | CLN5 | 1203 | CLN5 intracellular trafficking protein | O75503 |
