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Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Alliance of Genome Resources
Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.
| Source | Last Updated |
|---|---|
| Alliance of Genome Resources | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References ▲ |
|---|---|---|---|---|---|---|---|---|
| DOID:0090139 | cortisone reductase deficiency | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:0090139 | cortisone reductase deficiency | HGNC:4795 | Homo sapiens (human) | 9563 | H6PD |
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| DOID:3587 | pancreatic ductal carcinoma | HGNC:7371 | Homo sapiens (human) | 10232 | MSLN |
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| DOID:7147 | ankylosing spondylitis | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:11981 | morbid obesity | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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| DOID:2394 | ovarian cancer | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:1612 | breast cancer | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:10763 | hypertension | RGD:2082 | Rattus norvegicus (Norway rat) | 25233 | Akt2 |
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| DOID:2043 | hepatitis B | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:11613 | hyperandrogenism | HGNC:6021 | Homo sapiens (human) | 3572 | IL6ST |
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| DOID:13603 | obstructive jaundice | RGD:3269 | Rattus norvegicus (Norway rat) | 25737 | Pcna |
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| DOID:12361 | Graves' disease | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:4989 | pancreatitis | HGNC:12663 | Homo sapiens (human) | 7412 | VCAM1 |
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| DOID:3310 | atopic dermatitis | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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| DOID:0050811 | congenital adrenal hyperplasia | HGNC:2600 | Homo sapiens (human) | 1589 | CYP21A2 |
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| DOID:10652 | Alzheimer's disease | HGNC:9232 | Homo sapiens (human) | 5465 | PPARA |
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| DOID:12449 | aplastic anemia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:10283 | prostate cancer | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:10024 | migraine with aura | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:14264 | benign neonatal seizures | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:11702 | dysgammaglobulinemia | HGNC:12572 | Homo sapiens (human) | 7374 | UNG |
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| DOID:10652 | Alzheimer's disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:1470 | major depressive disorder | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:3393 | coronary artery disease | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:8677 | perinatal necrotizing enterocolitis | HGNC:9053 | Homo sapiens (human) | 5329 | PLAUR |
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