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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:0112127 | HRPT-related hyperuricemia | MGI:96217 | Mus musculus (house mouse) | 15452 | Hprt1 |
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| 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:9261 | nasopharynx carcinoma | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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| DOID:9452 | steatotic liver disease | SGD:S000003222 | Saccharomyces cerevisiae S288C | 852639 | HXK2 |
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| DOID:684 | hepatocellular carcinoma | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:635 | acquired immunodeficiency syndrome | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:850 | lung disease | MGI:105383 | Mus musculus (house mouse) | 16182 | Il18r1 |
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| DOID:6000 | congestive heart failure | RGD:620330 | Rattus norvegicus (Norway rat) | 170587 | Cs |
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| DOID:8986 | narcolepsy | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:3312 | bipolar disorder | HGNC:4092 | Homo sapiens (human) | 2571 | GAD1 |
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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:0080410 | familial adenomatous polyposis 2 | HGNC:7527 | Homo sapiens (human) | 4595 | MUTYH |
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