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 ▼ |
---|---|---|---|---|---|
C0919267 | ovarian neoplasm | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C0410207 | Tubular Aggregate Myopathy | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C0007137 | Squamous cell carcinoma | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C0025202 | melanoma | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C0151744 | Myocardial Ischemia | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C1140680 | Malignant neoplasm of ovary | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C0019693 | HIV Infections | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C4721610 | Carcinoma, Ovarian Epithelial | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C0007847 | Malignant tumor of cervix | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C0079774 | Peripheral T-Cell Lymphoma | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C0002736 | Amyotrophic Lateral Sclerosis | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C0085084 | Motor Neuron Disease | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C2239176 | Liver carcinoma | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C0206623 | Adenosquamous carcinoma | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C0003873 | Rheumatoid Arthritis | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C0005586 | Bipolar Disorder | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C0036341 | Schizophrenia | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C1834582 | MYELOPROLIFERATIVE SYNDROME, TRANSIENT | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C4048328 | cervical cancer | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C0524851 | Neurodegenerative Disorders | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C0019623 | Malignant histiocytosis | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C0302592 | Cervix carcinoma | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C0007570 | Celiac Disease | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C0152230 | Cholinergic urticaria | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
C0011603 | Dermatitis | CLEC10A | 10462 | C-type lectin domain containing 10A | Q8IUN9 |
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Last updated: August 19, 2024