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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:162 | cancer | Xenbase:XB-GENE-961670 | Xenopus tropicalis (tropical clawed frog) | 496958 | ppp1cb |
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| DOID:0080693 | Noonan syndrome-like disorder with loose anagen hair 2 | Xenbase:XB-GENE-961670 | Xenopus tropicalis (tropical clawed frog) | 496958 | ppp1cb |
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| DOID:206 | hereditary multiple exostoses | ZFIN:ZDB-GENE-050211-3 | Danio rerio (zebrafish) | 497279 | ext1a |
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| DOID:0060041 | autism spectrum disorder | ZFIN:ZDB-GENE-050211-3 | Danio rerio (zebrafish) | 497279 | ext1a |
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| DOID:3371 | chondrosarcoma | ZFIN:ZDB-GENE-050211-3 | Danio rerio (zebrafish) | 497279 | ext1a |
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| DOID:206 | hereditary multiple exostoses | ZFIN:ZDB-GENE-050211-4 | Danio rerio (zebrafish) | 497280 | ext1b |
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| DOID:3371 | chondrosarcoma | ZFIN:ZDB-GENE-050211-4 | Danio rerio (zebrafish) | 497280 | ext1b |
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| DOID:0060041 | autism spectrum disorder | ZFIN:ZDB-GENE-050211-4 | Danio rerio (zebrafish) | 497280 | ext1b |
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| DOID:206 | hereditary multiple exostoses | ZFIN:ZDB-GENE-050211-5 | Danio rerio (zebrafish) | 497281 | ext1c |
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| DOID:5844 | myocardial infarction | HGNC:8133 | Homo sapiens (human) | 4973 | OLR1 |
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| DOID:783 | end stage renal disease | HGNC:8133 | Homo sapiens (human) | 4973 | OLR1 |
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| DOID:9246 | cerebral amyloid angiopathy | HGNC:8133 | Homo sapiens (human) | 4973 | OLR1 |
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| DOID:3393 | coronary artery disease | HGNC:8133 | Homo sapiens (human) | 4973 | OLR1 |
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| DOID:10763 | hypertension | HGNC:8133 | Homo sapiens (human) | 4973 | OLR1 |
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| DOID:0112382 | muscular dystrophy-dystroglycanopathy type C8 | ZFIN:ZDB-GENE-050522-242 | Danio rerio (zebrafish) | 497644 | pomgnt2 |
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| DOID:0111231 | congenital muscular dystrophy-dystroglycanopathy type A8 | ZFIN:ZDB-GENE-050522-242 | Danio rerio (zebrafish) | 497644 | pomgnt2 |
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| DOID:2394 | ovarian cancer | HGNC:8143 | Homo sapiens (human) | 4978 | OPCML |
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| DOID:4752 | multiple system atrophy | RGD:1306722 | Rattus norvegicus (Norway rat) | 498332 | Coq2 |
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| DOID:0050730 | coenzyme Q10 deficiency disease | RGD:1306722 | Rattus norvegicus (Norway rat) | 498332 | Coq2 |
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| DOID:0070238 | primary coenzyme Q10 deficiency 1 | RGD:1306722 | Rattus norvegicus (Norway rat) | 498332 | Coq2 |
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| DOID:1184 | nephrotic syndrome | RGD:1306722 | Rattus norvegicus (Norway rat) | 498332 | Coq2 |
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| DOID:10603 | glucose intolerance | RGD:1306722 | Rattus norvegicus (Norway rat) | 498332 | Coq2 |
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| DOID:0081097 | Rafiq syndrome | RGD:1563595 | Rattus norvegicus (Norway rat) | 499751 | Man1b1 |
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| DOID:331 | central nervous system disease | HGNC:118 | Homo sapiens (human) | 50 | ACO2 |
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| DOID:0111442 | optic atrophy 9 | HGNC:118 | Homo sapiens (human) | 50 | ACO2 |
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