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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:1612 | breast cancer | HGNC:16049 | Homo sapiens (human) | 10728 | PTGES3 |
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| DOID:070355 | multisystem proteinopathy | MGI:2147627 | Mus musculus (house mouse) | 107271 | Yars1 |
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| DOID:0110199 | Charcot-Marie-Tooth disease dominant intermediate C | MGI:2147627 | Mus musculus (house mouse) | 107271 | Yars1 |
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| DOID:870 | neuropathy | MGI:2147627 | Mus musculus (house mouse) | 107271 | Yars1 |
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| DOID:10595 | Charcot-Marie-Tooth disease | MGI:2147627 | Mus musculus (house mouse) | 107271 | Yars1 |
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| DOID:162 | cancer | MGI:2147627 | Mus musculus (house mouse) | 107271 | Yars1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:7056 | Homo sapiens (human) | 10724 | OGA |
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| DOID:1826 | epilepsy | HGNC:10915 | Homo sapiens (human) | 10723 | SLC12A7 |
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| DOID:1184 | nephrotic syndrome | HGNC:1874 | Homo sapiens (human) | 1072 | CFL1 |
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| DOID:767 | muscular atrophy | HGNC:1874 | Homo sapiens (human) | 1072 | CFL1 |
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| DOID:0050562 | West syndrome | HGNC:1874 | Homo sapiens (human) | 1072 | CFL1 |
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| DOID:4948 | gallbladder carcinoma | HGNC:1874 | Homo sapiens (human) | 1072 | CFL1 |
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| DOID:5844 | myocardial infarction | HGNC:1874 | Homo sapiens (human) | 1072 | CFL1 |
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| DOID:1824 | status epilepticus | HGNC:1874 | Homo sapiens (human) | 1072 | CFL1 |
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| DOID:11457 | brain compression | HGNC:1874 | Homo sapiens (human) | 1072 | CFL1 |
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| DOID:5199 | ureteral obstruction | HGNC:1874 | Homo sapiens (human) | 1072 | CFL1 |
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| DOID:0050731 | vitamin B12 deficiency | HGNC:1874 | Homo sapiens (human) | 1072 | CFL1 |
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| DOID:0110934 | nemaline myopathy 7 | HGNC:1874 | Homo sapiens (human) | 1072 | CFL1 |
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| DOID:0060041 | autism spectrum disorder | HGNC:1874 | Homo sapiens (human) | 1072 | CFL1 |
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| DOID:1574 | alcohol use disorder | HGNC:1874 | Homo sapiens (human) | 1072 | CFL1 |
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| DOID:1875 | impotence | HGNC:1874 | Homo sapiens (human) | 1072 | CFL1 |
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| DOID:5419 | schizophrenia | HGNC:7999 | Homo sapiens (human) | 10718 | NRG3 |
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| DOID:0060041 | autism spectrum disorder | HGNC:11590 | Homo sapiens (human) | 10716 | TBR1 |
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| DOID:0111451 | progressive myoclonus epilepsy 8 | HGNC:14253 | Homo sapiens (human) | 10715 | CERS1 |
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| DOID:0111369 | hyperalphalipoproteinemia 1 | HGNC:1869 | Homo sapiens (human) | 1071 | CETP |
|
