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GlyTouCan
Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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MIRAGE
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 | January 28, 2025 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence | References ▲ |
|---|---|---|---|---|---|---|---|---|
| DOID:14365 | systemic primary carnitine deficiency disease | MGI:1329012 | Mus musculus (house mouse) | 20520 | Slc22a5 | author statement supported by traceable reference |
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| DOID:0110078 | Leber congenital amaurosis 1 | MGI:105123 | Mus musculus (house mouse) | 14919 | Gucy2e | author statement supported by traceable reference |
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| DOID:0110918 | hereditary spherocytosis type 3 | MGI:98385 | Mus musculus (house mouse) | 20739 | Spta1 | author statement supported by traceable reference |
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| DOID:0110916 | hereditary spherocytosis type 1 | MGI:98385 | Mus musculus (house mouse) | 20739 | Spta1 | author statement supported by traceable reference |
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| DOID:0050545 | visceral heterotaxy | MGI:106676 | Mus musculus (house mouse) | 22773 | Zic3 | author statement supported by traceable reference |
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| DOID:0080599 | Coronavirus infectious disease | MGI:2153525 | Mus musculus (house mouse) | 140474 | Muc4 | author statement supported by traceable reference |
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| DOID:11105 | fundus albipunctatus | MGI:2385957 | Mus musculus (house mouse) | 259172 | Mfrp | author statement supported by traceable reference |
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| DOID:0110867 | congenital stationary night blindness 1C | MGI:1330305 | Mus musculus (house mouse) | 17364 | Trpm1 | author statement supported by traceable reference |
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| DOID:9074 | systemic lupus erythematosus | MGI:95484 | Mus musculus (house mouse) | 14102 | Fas | author statement supported by traceable reference |
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| DOID:6688 | autoimmune lymphoproliferative syndrome | MGI:95484 | Mus musculus (house mouse) | 14102 | Fas | author statement supported by traceable reference |
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| DOID:6688 | autoimmune lymphoproliferative syndrome | MGI:99255 | Mus musculus (house mouse) | 14103 | Fasl | author statement supported by traceable reference |
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| DOID:4480 | achondroplasia | MGI:99602 | Mus musculus (house mouse) | 11595 | Acan | author statement supported by traceable reference |
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| DOID:0090140 | cortisone reductase deficiency 2 | MGI:103562 | Mus musculus (house mouse) | 15483 | Hsd11b1 | author statement supported by traceable reference |
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| DOID:2671 | transitional cell carcinoma | HGNC:1681 | Homo sapiens (human) | 960 | CD44 | direct assay evidence used in manual assertion |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:10446 | Homo sapiens (human) | 6236 | RRAD | inference by association of genotype from phenotype used in manual assertion |
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| DOID:11198 | DiGeorge syndrome | HGNC:12520 | Homo sapiens (human) | 7353 | UFD1 | inference by association of genotype from phenotype used in manual assertion |
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| DOID:10763 | hypertension | HGNC:2592 | Homo sapiens (human) | 1585 | CYP11B2 | inference by association of genotype from phenotype used in manual assertion |
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| DOID:2870 | endometrial adenocarcinoma | HGNC:15971 | Homo sapiens (human) | 7251 | TSG101 | direct assay evidence used in manual assertion |
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| DOID:10652 | Alzheimer's disease | HGNC:613 | Homo sapiens (human) | 348 | APOE | inference by association of genotype from phenotype used in manual assertion |
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| DOID:13994 | cleidocranial dysplasia | MGI:99829 | Mus musculus (house mouse) | 12393 | Runx2 | author statement supported by traceable reference |
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| DOID:2841 | asthma | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 | inference by association of genotype from phenotype used in manual assertion |
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| DOID:2841 | asthma | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 | inference by association of genotype from phenotype used in manual assertion |
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| DOID:12308 | Dubin-Johnson syndrome | HGNC:53 | Homo sapiens (human) | 1244 | ABCC2 | inference by association of genotype from phenotype used in manual assertion |
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| DOID:5212 | congenital disorder of glycosylation | HGNC:9115 | Homo sapiens (human) | 5373 | PMM2 | inference by association of genotype from phenotype used in manual assertion |
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| DOID:1064 | cystinosis | HGNC:2518 | Homo sapiens (human) | 1497 | CTNS | inference by association of genotype from phenotype used in manual assertion |
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