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 |
---|---|---|---|---|---|
C3714756 | Intellectual Disability | PLCH2 | 9651 | phospholipase C eta 2 | O75038 |
C0004509 | Azoospermia | PLCH2 | 9651 | phospholipase C eta 2 | O75038 |
C3554460 | COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 | PLCH1 | 23007 | phospholipase C eta 1 | Q4KWH8 |
C1319315 | Adenocarcinoma of large intestine | PLCH1 | 23007 | phospholipase C eta 1 | Q4KWH8 |
C0007102 | Malignant tumor of colon | PLCH1 | 23007 | phospholipase C eta 1 | Q4KWH8 |
C0242379 | Malignant neoplasm of lung | PLCH1 | 23007 | phospholipase C eta 1 | Q4KWH8 |
C0007131 | Non-Small Cell Lung Carcinoma | PLCH1 | 23007 | phospholipase C eta 1 | Q4KWH8 |
C1837461 | SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 | PLCH1 | 23007 | phospholipase C eta 1 | Q4KWH8 |
C0684249 | Carcinoma of lung | PLCH1 | 23007 | phospholipase C eta 1 | Q4KWH8 |
C0007137 | Squamous cell carcinoma | PLCH1 | 23007 | phospholipase C eta 1 | Q4KWH8 |
C0349631 | Richter's syndrome | PLCG2 | 5336 | phospholipase C gamma 2 | P16885 |
C3280914 | FAMILIAL COLD AUTOINFLAMMATORY SYNDROME 3 | PLCG2 | 5336 | phospholipase C gamma 2 | P16885 |
C0276496 | Familial Alzheimer Disease (FAD) | PLCG2 | 5336 | phospholipase C gamma 2 | P16885 |
C0023434 | Chronic Lymphocytic Leukemia | PLCG2 | 5336 | phospholipase C gamma 2 | P16885 |
C1332201 | Adult Diffuse Large B-Cell Lymphoma | PLCG2 | 5336 | phospholipase C gamma 2 | P16885 |
C0021390 | Inflammatory Bowel Diseases | PLCG2 | 5336 | phospholipase C gamma 2 | P16885 |
C1332986 | Childhood Osteosarcoma | PLCG2 | 5336 | phospholipase C gamma 2 | P16885 |
C0002395 | Alzheimer's Disease | PLCG2 | 5336 | phospholipase C gamma 2 | P16885 |
C0750901 | Alzheimer Disease, Early Onset | PLCG2 | 5336 | phospholipase C gamma 2 | P16885 |
C1861172 | Venous Thromboembolism | PLCG2 | 5336 | phospholipase C gamma 2 | P16885 |
C0409818 | Chronic Infantile Neurological, Cutaneous, and Articular Syndrome | PLCG2 | 5336 | phospholipase C gamma 2 | P16885 |
C0006142 | Malignant neoplasm of breast | PLCG2 | 5336 | phospholipase C gamma 2 | P16885 |
C0004364 | Autoimmune Diseases | PLCG2 | 5336 | phospholipase C gamma 2 | P16885 |
C0524851 | Neurodegenerative Disorders | PLCG2 | 5336 | phospholipase C gamma 2 | P16885 |
C0006826 | Malignant Neoplasms | PLCG2 | 5336 | phospholipase C gamma 2 | P16885 |
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Last updated: August 19, 2024