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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:2129 | atypical teratoid rhabdoid tumor | HGNC:4451 | Homo sapiens (human) | 2719 | GPC3 |
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| DOID:3596 | placental site trophoblastic tumor | HGNC:4451 | Homo sapiens (human) | 2719 | GPC3 |
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| DOID:687 | hepatoblastoma | HGNC:4451 | Homo sapiens (human) | 2719 | GPC3 |
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| DOID:0080844 | omodysplasia 1 | HGNC:4454 | Homo sapiens (human) | 10082 | GPC6 |
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| DOID:0110219 | Brugada syndrome 2 | SGD:S000002180 | Saccharomyces cerevisiae S288C | 851539 | GPD1 |
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| DOID:0110219 | Brugada syndrome 2 | HGNC:28956 | Homo sapiens (human) | 23171 | GPD1L |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:4456 | Homo sapiens (human) | 2820 | GPD2 |
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| DOID:0110219 | Brugada syndrome 2 | SGD:S000005420 | Saccharomyces cerevisiae S288C | 854095 | GPD2 |
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| DOID:13580 | cholestasis | SGD:S000006364 | Saccharomyces cerevisiae S288C | 856289 | GPH1 |
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| DOID:3650 | lactic acidosis | SGD:S000006364 | Saccharomyces cerevisiae S288C | 856289 | GPH1 |
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| DOID:2747 | glycogen storage disease | SGD:S000006364 | Saccharomyces cerevisiae S288C | 856289 | GPH1 |
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| DOID:2746 | glycogen storage disease V | SGD:S000006364 | Saccharomyces cerevisiae S288C | 856289 | GPH1 |
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| DOID:2754 | glycogen storage disease VI | SGD:S000006364 | Saccharomyces cerevisiae S288C | 856289 | GPH1 |
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| DOID:2861 | congenital nonspherocytic hemolytic anemia | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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| DOID:14330 | Parkinson's disease | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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| DOID:9119 | acute myeloid leukemia | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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| DOID:589 | congenital hemolytic anemia | 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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| DOID:114 | heart disease | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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| DOID:1059 | intellectual disability | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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| DOID:0112213 | multiple congenital anomalies-hypotonia-seizures syndrome 4 | SGD:S000003448 | Saccharomyces cerevisiae S288C | 853130 | GPI1 |
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| DOID:10112 | sleeping sickness | SGD:S000003110 | Saccharomyces cerevisiae S288C | 852735 | GPI10 |
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| DOID:0112216 | developmental and epileptic encephalopathy 80 | SGD:S000003110 | Saccharomyces cerevisiae S288C | 852735 | GPI10 |
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| DOID:0070433 | hyperphosphatasia with impaired intellectual development syndrome 1 | SGD:S000000208 | Saccharomyces cerevisiae S288C | 852289 | GPI18 |
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