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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:5517 | stomach carcinoma | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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| DOID:4483 | rhinitis | MGI:1341296 | Mus musculus (house mouse) | 21899 | Tlr6 |
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| DOID:13025 | retinopathy of prematurity | HGNC:3416 | Homo sapiens (human) | 2057 | EPOR |
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| DOID:0050827 | rheumatic heart disease | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:4483 | rhinitis | HGNC:7809 | Homo sapiens (human) | 4804 | NGFR |
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| DOID:0050156 | idiopathic pulmonary fibrosis | MGI:98736 | Mus musculus (house mouse) | 21824 | Thbd |
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| DOID:0050328 | congenital hypothyroidism | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:0110084 | arrhythmogenic right ventricular dysplasia 13 | HGNC:2511 | Homo sapiens (human) | 29119 | CTNNA3 |
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| DOID:0050793 | short QT syndrome | HGNC:18862 | Homo sapiens (human) | 81033 | KCNH6 |
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| DOID:13258 | typhoid fever | HGNC:6709 | Homo sapiens (human) | 4049 | LTA |
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| DOID:0080918 | polymicrogyria | HGNC:20768 | Homo sapiens (human) | 84790 | TUBA1C |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:3541 | Homo sapiens (human) | 2152 | F3 |
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| DOID:224 | transient cerebral ischemia | HGNC:2438 | Homo sapiens (human) | 1440 | CSF3 |
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| DOID:3068 | glioblastoma | MGI:97798 | Mus musculus (house mouse) | 19225 | Ptgs2 |
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| DOID:5844 | myocardial infarction | MGI:97610 | Mus musculus (house mouse) | 18791 | Plat |
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| DOID:1574 | alcohol use disorder | MGI:104771 | Mus musculus (house mouse) | 13869 | Erbb4 |
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| DOID:0080202 | adenoid cystic carcinoma | HGNC:12836 | Homo sapiens (human) | 22803 | XRN2 |
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| DOID:1702 | ichthyosis vulgaris | HGNC:3748 | Homo sapiens (human) | 2312 | FLG |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | SGD:S000002851 | Saccharomyces cerevisiae S288C | 852053 | SSN2 |
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| DOID:0060688 | arteriovenous malformations of the brain | WB:WBGene00000897 | Caenorhabditis elegans | 176829 | daf-1 |
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| DOID:783 | end stage renal disease | MGI:99454 | Mus musculus (house mouse) | 16367 | Irs1 |
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| DOID:0070302 | multiple epiphyseal dysplasia 7 | WB:WBGene00017244 | Caenorhabditis elegans | 181019 | apy-1 |
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| DOID:11832 | visual epilepsy | HGNC:5232 | Homo sapiens (human) | 3303 | HSPA1A |
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| DOID:11612 | polycystic ovary syndrome | HGNC:278 | Homo sapiens (human) | 147 | ADRA1B |
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| DOID:0050127 | sinusitis | HGNC:5973 | Homo sapiens (human) | 3596 | IL13 |
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