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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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Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID ▼ | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:1459 | hypothyroidism | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:0112195 | spondyloperipheral dysplasia | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:5614 | eye disease | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:0080056 | achondrogenesis type II | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:0080028 | spondyloepimetaphyseal dysplasia, Strudwick type | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:1574 | alcohol use disorder | HGNC:253 | Homo sapiens (human) | 128 | ADH5 |
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| DOID:0080952 | AMED syndrome | HGNC:253 | Homo sapiens (human) | 128 | ADH5 |
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| DOID:2841 | asthma | HGNC:253 | Homo sapiens (human) | 128 | ADH5 |
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| DOID:13580 | cholestasis | HGNC:253 | Homo sapiens (human) | 128 | ADH5 |
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| DOID:0050425 | restless legs syndrome | MGI:88437 | Mus musculus (house mouse) | 12799 | Cnp |
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| DOID:0112153 | hypomyelinating leukodystrophy 20 | MGI:88437 | Mus musculus (house mouse) | 12799 | Cnp |
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| DOID:2377 | multiple sclerosis | MGI:88437 | Mus musculus (house mouse) | 12799 | Cnp |
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| DOID:14018 | alcoholic liver cirrhosis | MGI:88437 | Mus musculus (house mouse) | 12799 | Cnp |
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| DOID:13001 | carotid stenosis | MGI:88437 | Mus musculus (house mouse) | 12799 | Cnp |
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| DOID:5419 | schizophrenia | MGI:88437 | Mus musculus (house mouse) | 12799 | Cnp |
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| DOID:0110007 | achromatopsia 2 | MGI:1341818 | Mus musculus (house mouse) | 12790 | Cnga3 |
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| DOID:13399 | color blindness | MGI:1341818 | Mus musculus (house mouse) | 12790 | Cnga3 |
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| DOID:0110377 | retinitis pigmentosa 49 | MGI:88436 | Mus musculus (house mouse) | 12788 | Cnga1 |
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| DOID:10584 | retinitis pigmentosa | MGI:88436 | Mus musculus (house mouse) | 12788 | Cnga1 |
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| DOID:439 | neuromuscular junction disease | HGNC:11510 | Homo sapiens (human) | 127833 | SYT2 |
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| DOID:0110659 | congenital myasthenic syndrome 7 | HGNC:11510 | Homo sapiens (human) | 127833 | SYT2 |
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| DOID:3635 | congenital myasthenic syndrome | HGNC:11510 | Homo sapiens (human) | 127833 | SYT2 |
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| DOID:1824 | status epilepticus | MGI:1352447 | Mus musculus (house mouse) | 12780 | Abcc2 |
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| DOID:1793 | pancreatic cancer | MGI:1352447 | Mus musculus (house mouse) | 12780 | Abcc2 |
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| DOID:11832 | visual epilepsy | MGI:1352447 | Mus musculus (house mouse) | 12780 | Abcc2 |
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