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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:9408 | acute myocardial infarction | RGD:735225 | Rattus norvegicus (Norway rat) | 295703 | Serping1 |
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| DOID:0080600 | COVID-19 | RGD:735225 | Rattus norvegicus (Norway rat) | 295703 | Serping1 |
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| DOID:3068 | glioblastoma | RGD:735225 | Rattus norvegicus (Norway rat) | 295703 | Serping1 |
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| DOID:898 | autosomal dominant polycystic kidney disease | RGD:735225 | Rattus norvegicus (Norway rat) | 295703 | Serping1 |
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| DOID:1558 | angioedema | RGD:735225 | Rattus norvegicus (Norway rat) | 295703 | Serping1 |
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| DOID:0080998 | acute necrotizing pancreatitis | RGD:735225 | Rattus norvegicus (Norway rat) | 295703 | Serping1 |
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| DOID:3526 | cerebral infarction | RGD:735225 | Rattus norvegicus (Norway rat) | 295703 | Serping1 |
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| DOID:2752 | glycogen storage disease II | RGD:735227 | Rattus norvegicus (Norway rat) | 367562 | Gaa |
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| DOID:0080411 | familial adenomatous polyposis 3 | SGD:S000000013 | Saccharomyces cerevisiae S288C | 851218 | NTG1 |
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| DOID:0111240 | congenital muscular dystrophy-dystroglycanopathy type A2 | SGD:S000000021 | Saccharomyces cerevisiae S288C | 851210 | PMT2 |
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| DOID:0112380 | muscular dystrophy-dystroglycanopathy type B2 | SGD:S000000021 | Saccharomyces cerevisiae S288C | 851210 | PMT2 |
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| DOID:0050560 | Walker-Warburg syndrome | SGD:S000000021 | Saccharomyces cerevisiae S288C | 851210 | PMT2 |
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| DOID:0050453 | lissencephaly | SGD:S000000021 | Saccharomyces cerevisiae S288C | 851210 | PMT2 |
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| DOID:0112374 | muscular dystrophy-dystroglycanopathy | SGD:S000000021 | Saccharomyces cerevisiae S288C | 851210 | PMT2 |
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| DOID:0110298 | autosomal recessive limb-girdle muscular dystrophy type 2N | SGD:S000000021 | Saccharomyces cerevisiae S288C | 851210 | PMT2 |
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| DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | SGD:S000000021 | Saccharomyces cerevisiae S288C | 851210 | PMT2 |
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| DOID:9884 | muscular dystrophy | SGD:S000000021 | Saccharomyces cerevisiae S288C | 851210 | PMT2 |
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| DOID:4195 | hyperglycemia | SGD:S000000036 | Saccharomyces cerevisiae S288C | 851193 | CDC19 |
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| DOID:0014667 | disease of metabolism | SGD:S000000036 | Saccharomyces cerevisiae S288C | 851193 | CDC19 |
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| DOID:10763 | hypertension | SGD:S000000036 | Saccharomyces cerevisiae S288C | 851193 | CDC19 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | SGD:S000000036 | Saccharomyces cerevisiae S288C | 851193 | CDC19 |
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| DOID:9970 | obesity | SGD:S000000054 | Saccharomyces cerevisiae S288C | 851241 | CNE1 |
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| DOID:0060269 | pontocerebellar hypoplasia type 2C | SGD:S000000066 | Saccharomyces cerevisiae S288C | 851267 | SEN34 |
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| DOID:3969 | thyroid gland papillary carcinoma | SGD:S000000094 | Saccharomyces cerevisiae S288C | 851299 | PHO11 |
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| DOID:0112333 | pontocerebellar hypoplasia type 16 | SGD:S000000094 | Saccharomyces cerevisiae S288C | 851299 | PHO11 |
|
