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 |
---|---|---|---|---|---|
C1332201 | Adult Diffuse Large B-Cell Lymphoma | CD109 | 135228 | CD109 molecule | Q6YHK3 |
C0410174 | Fukuyama Type Congenital Muscular Dystrophy | CD109 | 135228 | CD109 molecule | Q6YHK3 |
C0555198 | Malignant Glioma | CD109 | 135228 | CD109 molecule | Q6YHK3 |
C0026848 | Myopathy | CD109 | 135228 | CD109 molecule | Q6YHK3 |
C0600139 | Prostate carcinoma | CD109 | 135228 | CD109 molecule | Q6YHK3 |
C0003873 | Rheumatoid Arthritis | CD109 | 135228 | CD109 molecule | Q6YHK3 |
C0376358 | Malignant neoplasm of prostate | CD109 | 135228 | CD109 molecule | Q6YHK3 |
C0205944 | Sarcoma, Epithelioid | CD109 | 135228 | CD109 molecule | Q6YHK3 |
C1176475 | Ductal Carcinoma | CD109 | 135228 | CD109 molecule | Q6YHK3 |
C0036341 | Schizophrenia | B3GAT2 | 135152 | beta-1,3-glucuronyltransferase 2 | Q9NPZ5 |
C0004763 | Barrett Esophagus | B3GAT2 | 135152 | beta-1,3-glucuronyltransferase 2 | Q9NPZ5 |
C1861172 | Venous Thromboembolism | B3GAT2 | 135152 | beta-1,3-glucuronyltransferase 2 | Q9NPZ5 |
C0023903 | Liver neoplasms | ACOT12 | 134526 | acyl-CoA thioesterase 12 | Q8WYK0 |
C2239176 | Liver carcinoma | ACOT12 | 134526 | acyl-CoA thioesterase 12 | Q8WYK0 |
C0024620 | Primary Malignant Liver Neoplasm | ACOT12 | 134526 | acyl-CoA thioesterase 12 | Q8WYK0 |
C0345904 | Malignant neoplasm of liver | ACOT12 | 134526 | acyl-CoA thioesterase 12 | Q8WYK0 |
C1858991 | Childhood Ataxia with Central Nervous System Hypomyelinization | ACOT12 | 134526 | acyl-CoA thioesterase 12 | Q8WYK0 |
C0023520 | Leukodystrophy | ACOT12 | 134526 | acyl-CoA thioesterase 12 | Q8WYK0 |
C0854795 | Resectable Malignant Liver Neoplasm | ACOT12 | 134526 | acyl-CoA thioesterase 12 | Q8WYK0 |
C0028754 | Obesity | GNPDA2 | 132789 | glucosamine-6-phosphate deaminase 2 | Q8TDQ7 |
C0524620 | Metabolic Syndrome X | GNPDA2 | 132789 | glucosamine-6-phosphate deaminase 2 | Q8TDQ7 |
C0020538 | Hypertensive disease | GNPDA2 | 132789 | glucosamine-6-phosphate deaminase 2 | Q8TDQ7 |
C0030567 | Parkinson Disease | GNPDA2 | 132789 | glucosamine-6-phosphate deaminase 2 | Q8TDQ7 |
C0007222 | Cardiovascular Diseases | GNPDA2 | 132789 | glucosamine-6-phosphate deaminase 2 | Q8TDQ7 |
C3179455 | Niemann-Pick Disease, Type C1 | GNPDA2 | 132789 | glucosamine-6-phosphate deaminase 2 | Q8TDQ7 |
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Last updated: August 19, 2024