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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:0110914 | infantile hypophosphatasia | SGD:S000002889 | Saccharomyces cerevisiae S288C | 852092 | PHO8 |
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| DOID:10652 | Alzheimer's disease | SGD:S000006125 | Saccharomyces cerevisiae S288C | 855897 | HRR25 |
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| DOID:0060556 | Kufor-Rakeb syndrome | MGI:1922022 | Mus musculus (house mouse) | 74772 | Atp13a2 |
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| DOID:3083 | chronic obstructive pulmonary disease | RGD:621320 | Rattus norvegicus (Norway rat) | 81687 | Mmp9 |
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| DOID:5844 | myocardial infarction | HGNC:17760 | Homo sapiens (human) | 54210 | TREM1 |
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| DOID:0060041 | autism spectrum disorder | FB:FBgn0013997 | Drosophila melanogaster (fruit fly) | 39387 | Nrx-IV |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | RGD:3645 | Rattus norvegicus (Norway rat) | 24770 | Ccl2 |
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| DOID:0110277 | autosomal recessive limb-girdle muscular dystrophy type 2C | HGNC:10809 | Homo sapiens (human) | 6445 | SGCG |
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| DOID:9268 | glycine encephalopathy | MGI:1341155 | Mus musculus (house mouse) | 104174 | Gldc |
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| DOID:0050741 | alcohol dependence | RGD:61818 | Rattus norvegicus (Norway rat) | 79246 | Htr3a |
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| DOID:0060041 | autism spectrum disorder | HGNC:3091 | Homo sapiens (human) | 1859 | DYRK1A |
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| DOID:1059 | intellectual disability | HGNC:3091 | Homo sapiens (human) | 1859 | DYRK1A |
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| DOID:0050700 | cardiomyopathy | HGNC:7876 | Homo sapiens (human) | 4846 | NOS3 |
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| DOID:1094 | attention deficit hyperactivity disorder | MGI:1098283 | Mus musculus (house mouse) | 18626 | Per1 |
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| DOID:0090143 | brachyolmia-amelogenesis imperfecta syndrome | MGI:1101355 | Mus musculus (house mouse) | 16998 | Ltbp3 |
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| DOID:14330 | Parkinson's disease | HGNC:11503 | Homo sapiens (human) | 8867 | SYNJ1 |
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| DOID:14330 | Parkinson's disease | HGNC:14581 | Homo sapiens (human) | 65018 | PINK1 |
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| DOID:0111196 | X-linked distal spinal muscular atrophy 3 | MGI:99400 | Mus musculus (house mouse) | 11977 | Atp7a |
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| DOID:1574 | alcohol use disorder | HGNC:7808 | Homo sapiens (human) | 4803 | NGF |
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| DOID:1574 | alcohol use disorder | HGNC:4232 | Homo sapiens (human) | 2668 | GDNF |
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| DOID:9452 | steatotic liver disease | MGI:104663 | Mus musculus (house mouse) | 16846 | Lep |
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| DOID:9970 | obesity | RGD:2411 | Rattus norvegicus (Norway rat) | 25419 | Crp |
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| DOID:224 | transient cerebral ischemia | HGNC:30092 | Homo sapiens (human) | 10135 | NAMPT |
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| DOID:0110165 | Charcot-Marie-Tooth disease type 2E | MGI:97313 | Mus musculus (house mouse) | 18039 | Nefl |
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| DOID:684 | hepatocellular carcinoma | HGNC:4187 | Homo sapiens (human) | 2638 | GC |
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