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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB ▲ | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:2739 | Gilbert syndrome | MGI:98898 | Mus musculus (house mouse) | 394436 | Ugt1a1 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:29013 | Homo sapiens (human) | 23274 | CLEC16A |
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| DOID:7998 | hyperthyroidism | SGD:S000000598 | Saccharomyces cerevisiae S288C | 850361 | CIT2 |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:0080750 | erythema nodosum | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:14503 | neuronal ceroid lipofuscinosis | HGNC:9326 | Homo sapiens (human) | 9374 | PPT2 |
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| DOID:1612 | breast cancer | FB:FBgn0027070 | Drosophila melanogaster (fruit fly) | 35139 | Ugt36E1 |
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| DOID:0080322 | polycystic kidney disease | ZFIN:ZDB-GENE-030131-6586 | Danio rerio (zebrafish) | 751635 | alg5 |
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| DOID:0070450 | mitochondrial DNA depletion syndrome 19 | HGNC:10980 | Homo sapiens (human) | 1468 | SLC25A10 |
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| DOID:5844 | myocardial infarction | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:0060041 | autism spectrum disorder | HGNC:7682 | Homo sapiens (human) | 9348 | NDST3 |
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| DOID:0050771 | pheochromocytoma | HGNC:10681 | Homo sapiens (human) | 6390 | SDHB |
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| DOID:234 | colon adenocarcinoma | HGNC:545 | Homo sapiens (human) | 310 | ANXA7 |
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| DOID:3012 | Li-Fraumeni syndrome | MGI:98834 | Mus musculus (house mouse) | 22059 | Trp53 |
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| DOID:2871 | endometrial carcinoma | HGNC:11755 | Homo sapiens (human) | 7031 | TFF1 |
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| DOID:1459 | hypothyroidism | HGNC:2594 | Homo sapiens (human) | 1588 | CYP19A1 |
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| DOID:0050559 | Fukuyama congenital muscular dystrophy | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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| DOID:9952 | acute lymphoblastic leukemia | Xenbase:XB-GENE-5962599 | Xenopus tropicalis (tropical clawed frog) | 549437 | abo.3 |
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| DOID:11476 | osteoporosis | MGI:1346865 | Mus musculus (house mouse) | 26416 | Mapk14 |
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| DOID:3319 | lymphangioleiomyomatosis | WB:WBGene00001683 | Caenorhabditis elegans | 174603 | gpd-1 |
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| DOID:8677 | perinatal necrotizing enterocolitis | RGD:2053 | Rattus norvegicus (Norway rat) | 25591 | Parp1 |
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| DOID:9588 | encephalitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:1826 | epilepsy | RGD:2661 | Rattus norvegicus (Norway rat) | 24383 | Gapdh |
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| DOID:0112374 | muscular dystrophy-dystroglycanopathy | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:2921 | glomerulonephritis | HGNC:6719 | Homo sapiens (human) | 4056 | LTC4S |
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