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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:583 | hemolytic anemia | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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| DOID:9744 | type 1 diabetes mellitus | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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| DOID:6713 | cerebrovascular disease | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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| DOID:9970 | obesity | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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| DOID:13413 | hepatic encephalopathy | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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| DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00007435 | Caenorhabditis elegans | 182392 | algn-6 |
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| DOID:0080555 | congenital disorder of glycosylation Ic | WB:WBGene00007435 | Caenorhabditis elegans | 182392 | algn-6 |
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| DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00007464 | Caenorhabditis elegans | 174542 | algn-8 |
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| DOID:0050770 | polycystic liver disease | WB:WBGene00007464 | Caenorhabditis elegans | 174542 | algn-8 |
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| DOID:0080560 | congenital disorder of glycosylation Ih | WB:WBGene00007464 | Caenorhabditis elegans | 174542 | algn-8 |
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| DOID:0080564 | congenital disorder of glycosylation Il | WB:WBGene00007556 | Caenorhabditis elegans | 174633 | algn-9 |
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| DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00007556 | Caenorhabditis elegans | 174633 | algn-9 |
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| DOID:3633 | beta-mannosidosis | WB:WBGene00007904 | Caenorhabditis elegans | 181517 | C33G3.4 |
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| DOID:0060050 | autoimmune disease of blood | WB:WBGene00008019 | Caenorhabditis elegans | 176455 | C38H2.2 |
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| DOID:0111458 | galactose epimerase deficiency | WB:WBGene00008132 | Caenorhabditis elegans | 173171 | gale-1 |
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| DOID:9870 | galactosemia | WB:WBGene00008132 | Caenorhabditis elegans | 173171 | gale-1 |
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| DOID:1588 | thrombocytopenia | WB:WBGene00008132 | Caenorhabditis elegans | 173171 | gale-1 |
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| DOID:0014667 | disease of metabolism | WB:WBGene00008230 | Caenorhabditis elegans | 179335 | pfk-1.2 |
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| DOID:2747 | glycogen storage disease | WB:WBGene00008230 | Caenorhabditis elegans | 179335 | pfk-1.2 |
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| DOID:11721 | glycogen storage disease VII | WB:WBGene00008230 | Caenorhabditis elegans | 179335 | pfk-1.2 |
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| DOID:0112315 | brain small vessel disease 3 | WB:WBGene00008426 | Caenorhabditis elegans | 3565069 | D2045.9 |
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| DOID:0060284 | paroxysmal nocturnal hemoglobinuria | WB:WBGene00008431 | Caenorhabditis elegans | 174386 | piga-1 |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | WB:WBGene00008431 | Caenorhabditis elegans | 174386 | piga-1 |
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| DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | WB:WBGene00008431 | Caenorhabditis elegans | 174386 | piga-1 |
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| DOID:0060892 | late onset Parkinson's disease | WB:WBGene00008706 | Caenorhabditis elegans | 178535 | gba-3 |
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