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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:332 | amyotrophic lateral sclerosis | MGI:2136419 | Mus musculus (house mouse) | 237868 | Sarm1 |
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| DOID:0080559 | congenital disorder of glycosylation Ig | MGI:2385025 | Mus musculus (house mouse) | 223774 | Alg12 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:9283 | Homo sapiens (human) | 5501 | PPP1CC |
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| DOID:11612 | polycystic ovary syndrome | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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| DOID:12894 | Sjogren's syndrome | MGI:104798 | Mus musculus (house mouse) | 21926 | Tnf |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:0111239 | congenital muscular dystrophy-dystroglycanopathy type A10 | RGD:1309356 | Rattus norvegicus (Norway rat) | 299841 | Rxylt1 |
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| DOID:2739 | Gilbert syndrome | FB:FBgn0036842 | Drosophila melanogaster (fruit fly) | 40079 | Ugt316A1 |
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| DOID:6000 | congestive heart failure | MGI:109354 | Mus musculus (house mouse) | 22228 | Ucp2 |
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| DOID:0050848 | obstructive sleep apnea | MGI:104798 | Mus musculus (house mouse) | 21926 | Tnf |
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| DOID:13317 | hyperinsulinemic hypoglycemia | SGD:S000003222 | Saccharomyces cerevisiae S288C | 852639 | HXK2 |
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| DOID:0060041 | autism spectrum disorder | HGNC:7680 | Homo sapiens (human) | 3340 | NDST1 |
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| DOID:3803 | Crigler-Najjar syndrome | SGD:S000004179 | Saccharomyces cerevisiae S288C | 850886 | ATG26 |
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| DOID:1826 | epilepsy | MGI:3036255 | Mus musculus (house mouse) | 237500 | Tmtc3 |
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| DOID:0080488 | mucolipidosis | MGI:3643902 | Mus musculus (house mouse) | 432486 | Gnptab |
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| DOID:0111238 | congenital muscular dystrophy-dystroglycanopathy type A13 | ZFIN:ZDB-GENE-121001-5 | Danio rerio (zebrafish) | 101669768 | b4gat1 |
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| DOID:5804 | discrete subaortic stenosis | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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| DOID:2945 | severe acute respiratory syndrome | MGI:2135738 | Mus musculus (house mouse) | 80908 | Abo |
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| DOID:10952 | nephritis | WB:WBGene00004049 | Caenorhabditis elegans | 266823 | parp-1 |
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| DOID:2527 | nephrosis | HGNC:2606 | Homo sapiens (human) | 1594 | CYP27B1 |
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| DOID:0060050 | autoimmune disease of blood | ZFIN:ZDB-GENE-060503-810 | Danio rerio (zebrafish) | 555344 | c1galt1a |
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| DOID:206 | hereditary multiple exostoses | RGD:62065 | Rattus norvegicus (Norway rat) | 56819 | Extl3 |
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| DOID:784 | chronic kidney disease | HGNC:6554 | Homo sapiens (human) | 3953 | LEPR |
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| DOID:9675 | pulmonary emphysema | HGNC:4311 | Homo sapiens (human) | 2729 | GCLC |
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| DOID:2945 | severe acute respiratory syndrome | Xenbase:XB-GENE-969944 | Xenopus tropicalis (tropical clawed frog) | 549858 | abo.2 |
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