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 ▲ |
---|---|---|---|---|---|
C0006826 | Malignant Neoplasms | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
C0002895 | Anemia, Sickle Cell | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
C0042373 | Vascular Diseases | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
C0011884 | Diabetic Retinopathy | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
C0013264 | Muscular Dystrophy, Duchenne | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
C0020538 | Hypertensive disease | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
C0015414 | Eye Neoplasms | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
C0019061 | Hemolytic-Uremic Syndrome | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
C0015934 | Fetal Growth Retardation | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
C0745103 | Hyperlipoproteinemia Type IIa | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
C0205851 | Germ cell tumor | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
C0004352 | Autistic Disorder | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
C0497327 | Dementia | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
C0678222 | Breast Carcinoma | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
C0002395 | Alzheimer's Disease | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
C0035335 | Retinoblastoma | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
C0220633 | Uveal melanoma | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
C0014175 | Endometriosis | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
C0796012 | Krause-Kivlin syndrome | B3GALT1 | 8708 | beta-1,3-galactosyltransferase 1 | Q9Y5Z6 |
C0001418 | Adenocarcinoma | B3GALT1 | 8708 | beta-1,3-galactosyltransferase 1 | Q9Y5Z6 |
C1850318 | Omodysplasia type 1 | GPC6 | 10082 | glypican 6 | Q9Y625 |
C0029456 | Osteoporosis | GPC6 | 10082 | glypican 6 | Q9Y625 |
C0158266 | Intervertebral Disc Degeneration | GPC6 | 10082 | glypican 6 | Q9Y625 |
C0019270 | Hernia | GPC6 | 10082 | glypican 6 | Q9Y625 |
C0677886 | Epithelial ovarian cancer | GPC6 | 10082 | glypican 6 | Q9Y625 |
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Last updated: August 19, 2024