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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:9970 | obesity | HGNC:13345 | Homo sapiens (human) | 23175 | LPIN1 |
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| DOID:783 | end stage renal disease | HGNC:13345 | Homo sapiens (human) | 23175 | LPIN1 |
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| DOID:0080322 | polycystic kidney disease | HGNC:4138 | Homo sapiens (human) | 23193 | GANAB |
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| DOID:0050770 | polycystic liver disease | HGNC:4138 | Homo sapiens (human) | 23193 | GANAB |
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| DOID:0110860 | polycystic kidney disease 3 | HGNC:4138 | Homo sapiens (human) | 23193 | GANAB |
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| DOID:10588 | adrenoleukodystrophy | HGNC:29567 | Homo sapiens (human) | 23205 | ACSBG1 |
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| DOID:10652 | Alzheimer's disease | HGNC:15917 | Homo sapiens (human) | 23236 | PLCB1 |
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| DOID:5844 | myocardial infarction | HGNC:15917 | Homo sapiens (human) | 23236 | PLCB1 |
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| DOID:0050908 | myelodysplastic syndrome | HGNC:15917 | Homo sapiens (human) | 23236 | PLCB1 |
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| DOID:0080459 | developmental and epileptic encephalopathy 12 | HGNC:15917 | Homo sapiens (human) | 23236 | PLCB1 |
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| DOID:5419 | schizophrenia | HGNC:15917 | Homo sapiens (human) | 23236 | PLCB1 |
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| DOID:9970 | obesity | HGNC:15917 | Homo sapiens (human) | 23236 | PLCB1 |
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| DOID:9119 | acute myeloid leukemia | HGNC:15917 | Homo sapiens (human) | 23236 | PLCB1 |
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| DOID:2747 | glycogen storage disease | MGI:2385254 | Mus musculus (house mouse) | 232493 | Gys2 |
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| DOID:3534 | Lafora disease | MGI:2385254 | Mus musculus (house mouse) | 232493 | Gys2 |
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| DOID:2377 | multiple sclerosis | HGNC:29013 | Homo sapiens (human) | 23274 | CLEC16A |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:29013 | Homo sapiens (human) | 23274 | CLEC16A |
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| DOID:13774 | Addison's disease | HGNC:29013 | Homo sapiens (human) | 23274 | CLEC16A |
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| DOID:7148 | rheumatoid arthritis | HGNC:29013 | Homo sapiens (human) | 23274 | CLEC16A |
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| DOID:1289 | neurodegenerative disease | HGNC:29013 | Homo sapiens (human) | 23274 | CLEC16A |
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| DOID:14250 | Down syndrome | HGNC:14683 | Homo sapiens (human) | 23275 | POFUT2 |
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| DOID:1826 | epilepsy | MGI:88107 | Mus musculus (house mouse) | 232975 | Atp1a3 |
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| DOID:0090056 | dystonia 12 | MGI:88107 | Mus musculus (house mouse) | 232975 | Atp1a3 |
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| DOID:3312 | bipolar disorder | MGI:88107 | Mus musculus (house mouse) | 232975 | Atp1a3 |
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| DOID:0050635 | alternating hemiplegia of childhood | MGI:88107 | Mus musculus (house mouse) | 232975 | Atp1a3 |
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