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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:10652 | Alzheimer's disease | HGNC:15917 | Homo sapiens (human) | 23236 | PLCB1 |
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| DOID:9352 | type 2 diabetes mellitus | MGI:1270854 | Mus musculus (house mouse) | 103988 | Gck |
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| DOID:2750 | glycogen storage disease IV | SGD:S000000737 | Saccharomyces cerevisiae S288C | 856705 | GLC3 |
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| DOID:2861 | congenital nonspherocytic hemolytic anemia | MGI:95797 | Mus musculus (house mouse) | 14751 | Gpi1 |
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| DOID:9266 | cystinuria | HGNC:11025 | Homo sapiens (human) | 6519 | SLC3A1 |
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| DOID:3320 | Tay-Sachs disease | MGI:96073 | Mus musculus (house mouse) | 15211 | Hexa |
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| DOID:0060246 | MASA syndrome | HGNC:6470 | Homo sapiens (human) | 3897 | L1CAM |
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| DOID:10908 | hydrocephalus | HGNC:6470 | Homo sapiens (human) | 3897 | L1CAM |
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| DOID:0050570 | congenital disorder of glycosylation type I | MGI:1859214 | Mus musculus (house mouse) | 54128 | Pmm2 |
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| DOID:0111040 | glycogen storage disease IXd | MGI:97576 | Mus musculus (house mouse) | 18679 | Phka1 |
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| DOID:9452 | steatotic liver disease | HGNC:4801 | Homo sapiens (human) | 3030 | HADHA |
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| DOID:0060284 | paroxysmal nocturnal hemoglobinuria | SGD:S000006096 | Saccharomyces cerevisiae S288C | 855928 | SPT14 |
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| DOID:9352 | type 2 diabetes mellitus | RGD:2303 | Rattus norvegicus (Norway rat) | 25668 | Cd38 |
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| DOID:5844 | myocardial infarction | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:3652 | Leigh disease | HGNC:10680 | Homo sapiens (human) | 6389 | SDHA |
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| DOID:12716 | newborn respiratory distress syndrome | HGNC:10802 | Homo sapiens (human) | 6440 | SFTPC |
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| DOID:12858 | Huntington's disease | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:14497 | Wolman disease | HGNC:6617 | Homo sapiens (human) | 3988 | LIPA |
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| DOID:0060202 | amyotrophic lateral sclerosis type 11 | SGD:S000005269 | Saccharomyces cerevisiae S288C | 855392 | FIG4 |
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| DOID:0080923 | bilateral parasagittal parieto-occipital polymicrogyria | SGD:S000005269 | Saccharomyces cerevisiae S288C | 855392 | FIG4 |
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| DOID:0060589 | Yunis-Varon syndrome | SGD:S000005269 | Saccharomyces cerevisiae S288C | 855392 | FIG4 |
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| DOID:13317 | hyperinsulinemic hypoglycemia | SGD:S000000545 | Saccharomyces cerevisiae S288C | 850317 | GLK1 |
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| DOID:0080507 | Cornelia de Lange syndrome 3 | FB:FBgn0015615 | Drosophila melanogaster (fruit fly) | 32627 | SMC3 |
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| DOID:0080562 | congenital disorder of glycosylation Ij | FB:FBgn0032477 | Drosophila melanogaster (fruit fly) | 34711 | Alg7 | CG5287 |
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| DOID:0111041 | glycogen storage disease IXb | MGI:97578 | Mus musculus (house mouse) | 102093 | Phkb |
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