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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:9256 | colorectal cancer | HGNC:4854 | Homo sapiens (human) | 8841 | HDAC3 |
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| DOID:4001 | ovarian carcinoma | HGNC:4854 | Homo sapiens (human) | 8841 | HDAC3 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:4854 | Homo sapiens (human) | 8841 | HDAC3 |
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| DOID:0070227 | intrahepatic cholestasis of pregnancy | HGNC:4854 | Homo sapiens (human) | 8841 | HDAC3 |
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| DOID:9351 | diabetes mellitus | HGNC:9454 | Homo sapiens (human) | 8842 | PROM1 |
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| DOID:0111019 | cone-rod dystrophy 12 | HGNC:9454 | Homo sapiens (human) | 8842 | PROM1 |
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| DOID:8466 | retinal degeneration | HGNC:9454 | Homo sapiens (human) | 8842 | PROM1 |
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| DOID:0110376 | retinitis pigmentosa 41 | HGNC:9454 | Homo sapiens (human) | 8842 | PROM1 |
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| DOID:0070517 | retinal macular dystrophy 2 | HGNC:9454 | Homo sapiens (human) | 8842 | PROM1 |
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| DOID:83 | cataract | HGNC:1569 | Homo sapiens (human) | 885 | CCK |
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| DOID:14330 | Parkinson's disease | HGNC:1569 | Homo sapiens (human) | 885 | CCK |
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| DOID:0050741 | alcohol dependence | HGNC:1569 | Homo sapiens (human) | 885 | CCK |
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| DOID:2913 | acute pancreatitis | HGNC:1569 | Homo sapiens (human) | 885 | CCK |
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| DOID:11981 | morbid obesity | HGNC:1569 | Homo sapiens (human) | 885 | CCK |
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| DOID:0050742 | nicotine dependence | HGNC:1569 | Homo sapiens (human) | 885 | CCK |
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| DOID:4988 | alcoholic pancreatitis | HGNC:1569 | Homo sapiens (human) | 885 | CCK |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:8638 | Homo sapiens (human) | 8850 | KAT2B |
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| DOID:1612 | breast cancer | HGNC:8638 | Homo sapiens (human) | 8850 | KAT2B |
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| DOID:114 | heart disease | HGNC:8638 | Homo sapiens (human) | 8850 | KAT2B |
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| DOID:684 | hepatocellular carcinoma | HGNC:8638 | Homo sapiens (human) | 8850 | KAT2B |
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| DOID:557 | kidney disease | HGNC:8638 | Homo sapiens (human) | 8850 | KAT2B |
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| DOID:7148 | rheumatoid arthritis | HGNC:8638 | Homo sapiens (human) | 8850 | KAT2B |
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| DOID:3827 | congenital diaphragmatic hernia | HGNC:15472 | Homo sapiens (human) | 8854 | ALDH1A2 |
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| DOID:11198 | DiGeorge syndrome | HGNC:15472 | Homo sapiens (human) | 8854 | ALDH1A2 |
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| DOID:9970 | obesity | HGNC:15472 | Homo sapiens (human) | 8854 | ALDH1A2 |
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