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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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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:9352 | type 2 diabetes mellitus | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:1612 | breast cancer | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:0110859 | polycystic kidney disease 2 | HGNC:9009 | Homo sapiens (human) | 5311 | PKD2 |
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| DOID:417 | autoimmune disease | HGNC:18187 | Homo sapiens (human) | 54414 | SIAE |
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| DOID:11446 | sciatic neuropathy | HGNC:2593 | Homo sapiens (human) | 1586 | CYP17A1 |
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| DOID:12716 | newborn respiratory distress syndrome | HGNC:10802 | Homo sapiens (human) | 6440 | SFTPC |
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| DOID:9206 | Barrett's esophagus | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:0050811 | congenital adrenal hyperplasia | HGNC:2600 | Homo sapiens (human) | 1589 | CYP21A2 |
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| DOID:3633 | beta-mannosidosis | HGNC:6831 | Homo sapiens (human) | 4126 | MANBA |
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| DOID:2394 | ovarian cancer | HGNC:1753 | Homo sapiens (human) | 1012 | CDH13 |
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| DOID:14067 | Plasmodium falciparum malaria | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:2977 | primary hyperoxaluria | HGNC:25155 | Homo sapiens (human) | 112817 | HOGA1 |
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| DOID:169 | neuroendocrine tumor | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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| DOID:3393 | coronary artery disease | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:8947 | diabetic retinopathy | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:13564 | aspergillosis | HGNC:24355 | Homo sapiens (human) | 51267 | CLEC1A |
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| DOID:0080736 | Ehlers-Danlos syndrome musculocontractural type 1 | HGNC:24464 | Homo sapiens (human) | 113189 | CHST14 |
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| DOID:14692 | Smith-Lemli-Opitz syndrome | HGNC:2860 | Homo sapiens (human) | 1717 | DHCR7 |
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| DOID:635 | acquired immunodeficiency syndrome | HGNC:1119 | Homo sapiens (human) | 684 | BST2 |
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| DOID:0060180 | colitis | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:9452 | steatotic liver disease | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:0060903 | thrombosis | HGNC:8976 | Homo sapiens (human) | 5291 | PIK3CB |
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| DOID:3450 | cutaneous Paget's disease | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:2349 | arteriosclerosis | HGNC:93 | Homo sapiens (human) | 38 | ACAT1 |
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| DOID:8778 | Crohn's disease | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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