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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 |
|---|---|---|---|---|---|
| C1609433 | Congenital absence of kidneys syndrome | HS6ST1 | 9394 | heparan sulfate 6-O-sulfotransferase 1 | O60243 |
| C0220748 | Cartilage-hair hypoplasia | HS6ST1 | 9394 | heparan sulfate 6-O-sulfotransferase 1 | O60243 |
| C0003467 | Anxiety | HS6ST1 | 9394 | heparan sulfate 6-O-sulfotransferase 1 | O60243 |
| C0018784 | Sensorineural Hearing Loss (disorder) | HS6ST1 | 9394 | heparan sulfate 6-O-sulfotransferase 1 | O60243 |
| C3665347 | Visual Impairment | HS6ST1 | 9394 | heparan sulfate 6-O-sulfotransferase 1 | O60243 |
| C0011849 | Diabetes Mellitus | HS6ST1 | 9394 | heparan sulfate 6-O-sulfotransferase 1 | O60243 |
| C0011581 | Depressive disorder | HS6ST1 | 9394 | heparan sulfate 6-O-sulfotransferase 1 | O60243 |
| C0005745 | Blepharoptosis | HS6ST1 | 9394 | heparan sulfate 6-O-sulfotransferase 1 | O60243 |
| C0030486 | Paraplegia | HS6ST1 | 9394 | heparan sulfate 6-O-sulfotransferase 1 | O60243 |
| C0028738 | Nystagmus | HS6ST1 | 9394 | heparan sulfate 6-O-sulfotransferase 1 | O60243 |
| C0010414 | Infection by Cryptococcus neoformans | CLEC6A | 93978 | C-type lectin domain containing 6A | Q6EIG7 |
| C0153252 | Systemic candidiasis | CLEC6A | 93978 | C-type lectin domain containing 6A | Q6EIG7 |
| C0042384 | Vasculitis | CLEC6A | 93978 | C-type lectin domain containing 6A | Q6EIG7 |
| C0010674 | Cystic Fibrosis | CLEC6A | 93978 | C-type lectin domain containing 6A | Q6EIG7 |
| C1306459 | Primary malignant neoplasm | CLEC6A | 93978 | C-type lectin domain containing 6A | Q6EIG7 |
| C0008373 | Cholesteatoma | CLEC6A | 93978 | C-type lectin domain containing 6A | Q6EIG7 |
| C0040247 | Tinea | CLEC6A | 93978 | C-type lectin domain containing 6A | Q6EIG7 |
| C0026691 | Mucocutaneous Lymph Node Syndrome | CLEC6A | 93978 | C-type lectin domain containing 6A | Q6EIG7 |
| C0003850 | Arteriosclerosis | CLEC6A | 93978 | C-type lectin domain containing 6A | Q6EIG7 |
| C0011636 | Dermatophytosis | CLEC6A | 93978 | C-type lectin domain containing 6A | Q6EIG7 |
| C0026946 | Mycoses | CLEC6A | 93978 | C-type lectin domain containing 6A | Q6EIG7 |
| C3714636 | Pneumonitis | CLEC6A | 93978 | C-type lectin domain containing 6A | Q6EIG7 |
| C0006826 | Malignant Neoplasms | CLEC6A | 93978 | C-type lectin domain containing 6A | Q6EIG7 |
| C0004153 | Atherosclerosis | CLEC6A | 93978 | C-type lectin domain containing 6A | Q6EIG7 |
| C0041296 | Tuberculosis | CLEC6A | 93978 | C-type lectin domain containing 6A | Q6EIG7 |
