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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:3211 | lysosomal storage disease | HGNC:10933 | Homo sapiens (human) | 26503 | SLC17A5 |
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| DOID:13580 | cholestasis | HGNC:2651 | Homo sapiens (human) | 1581 | CYP7A1 |
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| DOID:9452 | steatotic liver disease | SGD:S000003222 | Saccharomyces cerevisiae S288C | 852639 | HXK2 |
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| DOID:850 | lung disease | MGI:105383 | Mus musculus (house mouse) | 16182 | Il18r1 |
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| DOID:11727 | facioscapulohumeral muscular dystrophy | WB:WBGene00010716 | Caenorhabditis elegans | 187206 | lge-1 |
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| DOID:12858 | Huntington's disease | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:27301 | Homo sapiens (human) | 200186 | CRTC2 |
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| DOID:11758 | iron deficiency anemia | MGI:104798 | Mus musculus (house mouse) | 21926 | Tnf |
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| DOID:1574 | alcohol use disorder | RGD:2168 | Rattus norvegicus (Norway rat) | 24212 | Atp1a2 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:6107 | Homo sapiens (human) | 3651 | PDX1 |
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| DOID:12858 | Huntington's disease | MGI:1914625 | Mus musculus (house mouse) | 67375 | Qprt |
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| DOID:8677 | perinatal necrotizing enterocolitis | MGI:1346060 | Mus musculus (house mouse) | 24088 | Tlr2 |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | ZFIN:ZDB-GENE-040426-1086 | Danio rerio (zebrafish) | 791759 | piga |
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| DOID:14067 | Plasmodium falciparum malaria | RGD:1311152 | Rattus norvegicus (Norway rat) | 296504 | Abo2 |
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| DOID:0050453 | lissencephaly | Xenbase:XB-GENE-959856 | Xenopus tropicalis (tropical clawed frog) | 100158594 | pomgnt1 |
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| DOID:14115 | toxic shock syndrome | MGI:95394 | Mus musculus (house mouse) | 13807 | Eno2 |
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| DOID:14735 | hereditary angioedema | RGD:1584381 | Rattus norvegicus (Norway rat) | 684979 | Hs3st6 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:3594 | Homo sapiens (human) | 2194 | FASN |
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| DOID:8466 | retinal degeneration | SGD:S000000598 | Saccharomyces cerevisiae S288C | 850361 | CIT2 |
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| DOID:4195 | hyperglycemia | MGI:104993 | Mus musculus (house mouse) | 16847 | Lepr |
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| DOID:2747 | glycogen storage disease | MGI:97577 | Mus musculus (house mouse) | 110094 | Phka2 |
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| DOID:0050770 | polycystic liver disease | WB:WBGene00007464 | Caenorhabditis elegans | 174542 | algn-8 |
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| DOID:13413 | hepatic encephalopathy | MGI:105977 | Mus musculus (house mouse) | 14380 | G6pd2 |
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| DOID:162 | cancer | RGD:1307107 | Rattus norvegicus (Norway rat) | 303872 | Pigz |
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