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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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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:9352 | type 2 diabetes mellitus | HGNC:2295 | Homo sapiens (human) | 1356 | CP |
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| DOID:2316 | brain ischemia | HGNC:2295 | Homo sapiens (human) | 1356 | CP |
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| DOID:0050711 | aceruloplasminemia | HGNC:2295 | Homo sapiens (human) | 1356 | CP |
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| DOID:1826 | epilepsy | HGNC:2295 | Homo sapiens (human) | 1356 | CP |
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| DOID:13580 | cholestasis | HGNC:2295 | Homo sapiens (human) | 1356 | CP |
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| DOID:418 | systemic scleroderma | HGNC:2295 | Homo sapiens (human) | 1356 | CP |
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| DOID:114 | heart disease | HGNC:2295 | Homo sapiens (human) | 1356 | CP |
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| DOID:893 | Wilson disease | HGNC:2295 | Homo sapiens (human) | 1356 | CP |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:2295 | Homo sapiens (human) | 1356 | CP |
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| DOID:12119 | hemosiderosis | HGNC:2295 | Homo sapiens (human) | 1356 | CP |
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| DOID:4724 | brain edema | HGNC:2295 | Homo sapiens (human) | 1356 | CP |
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| DOID:3762 | cytochrome-c oxidase deficiency disease | HGNC:16232 | Homo sapiens (human) | 84701 | COX4I2 |
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| DOID:0070485 | mitochondrial complex IV deficiency nuclear type 23 | HGNC:2261 | Homo sapiens (human) | 1353 | COX11 |
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| DOID:3762 | cytochrome-c oxidase deficiency disease | RGD:621871 | Rattus norvegicus (Norway rat) | 26195 | COX1 |
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| DOID:0080855 | Parkinsonism | MGI:102504 | Mus musculus (house mouse) | 17708 | COX1 |
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| DOID:0080855 | Parkinsonism | RGD:621871 | Rattus norvegicus (Norway rat) | 26195 | COX1 |
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| DOID:3762 | cytochrome-c oxidase deficiency disease | HGNC:7419 | Homo sapiens (human) | 4512 | COX1 |
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| DOID:684 | hepatocellular carcinoma | MGI:102504 | Mus musculus (house mouse) | 17708 | COX1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:7419 | Homo sapiens (human) | 4512 | COX1 |
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| DOID:3762 | cytochrome-c oxidase deficiency disease | MGI:102504 | Mus musculus (house mouse) | 17708 | COX1 |
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| DOID:684 | hepatocellular carcinoma | RGD:621871 | Rattus norvegicus (Norway rat) | 26195 | COX1 |
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| DOID:0080855 | Parkinsonism | HGNC:7419 | Homo sapiens (human) | 4512 | COX1 |
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| DOID:9970 | obesity | HGNC:26161 | Homo sapiens (human) | 79585 | CORO7 |
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| DOID:13207 | proliferative diabetic retinopathy | HGNC:2254 | Homo sapiens (human) | 23603 | CORO1C |
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| DOID:0090014 | severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive | HGNC:2252 | Homo sapiens (human) | 11151 | CORO1A |
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