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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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References ▲ |
|---|---|---|---|---|---|---|---|---|
| DOID:10534 | stomach cancer | HGNC:3689 | Homo sapiens (human) | 2263 | FGFR2 |
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| DOID:2377 | multiple sclerosis | HGNC:5438 | Homo sapiens (human) | 3458 | IFNG |
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| DOID:0060870 | isolated growth hormone deficiency | RGD:621397 | Rattus norvegicus (Norway rat) | 84022 | Ghsr |
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| DOID:11573 | listeriosis | RGD:2887 | Rattus norvegicus (Norway rat) | 25670 | Il15 |
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| DOID:13406 | pulmonary sarcoidosis | HGNC:4540 | Homo sapiens (human) | 2833 | CXCR3 |
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| DOID:13241 | Behcet's disease | HGNC:11920 | Homo sapiens (human) | 355 | FAS |
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| DOID:9744 | type 1 diabetes mellitus | RGD:3935 | Rattus norvegicus (Norway rat) | 24861 | Ugt1a1 |
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| DOID:627 | severe combined immunodeficiency | HGNC:6024 | Homo sapiens (human) | 3575 | IL7R |
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| DOID:2986 | IgA glomerulonephritis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:11713 | diabetic angiopathy | HGNC:8583 | Homo sapiens (human) | 5054 | SERPINE1 |
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| DOID:13375 | temporal arteritis | HGNC:2434 | Homo sapiens (human) | 1437 | CSF2 |
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| DOID:7147 | ankylosing spondylitis | HGNC:5472 | Homo sapiens (human) | 3486 | IGFBP3 |
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| DOID:0050426 | Stevens-Johnson syndrome | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:1687 | neovascular glaucoma | HGNC:12680 | Homo sapiens (human) | 7422 | VEGFA |
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| DOID:3049 | Churg-Strauss syndrome | HGNC:4232 | Homo sapiens (human) | 2668 | GDNF |
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| DOID:12842 | Guillain-Barre syndrome | HGNC:4232 | Homo sapiens (human) | 2668 | GDNF |
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| DOID:9810 | polyarteritis nodosa | HGNC:4243 | Homo sapiens (human) | 2674 | GFRA1 |
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| DOID:9810 | polyarteritis nodosa | HGNC:4232 | Homo sapiens (human) | 2668 | GDNF |
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| DOID:12894 | Sjogren's syndrome | HGNC:4232 | Homo sapiens (human) | 2668 | GDNF |
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| DOID:3049 | Churg-Strauss syndrome | HGNC:4243 | Homo sapiens (human) | 2674 | GFRA1 |
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| DOID:0080379 | nephrotic syndrome type 2 | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
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| DOID:0060859 | salmonellosis | HGNC:5970 | Homo sapiens (human) | 3593 | IL12B |
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| DOID:9667 | placental abruption | HGNC:9451 | Homo sapiens (human) | 5624 | PROC |
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| DOID:1059 | intellectual disability | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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| DOID:440 | neuromuscular disease | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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