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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:0050741 | alcohol dependence | HGNC:2345 | Homo sapiens (human) | 1385 | CREB1 |
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| DOID:5419 | schizophrenia | HGNC:17328 | Homo sapiens (human) | 84062 | DTNBP1 |
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| DOID:0060793 | hypomyelinating leukodystrophy 5 | HGNC:24587 | Homo sapiens (human) | 84668 | HYCC1 |
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| DOID:10763 | hypertension | HGNC:243 | Homo sapiens (human) | 118 | ADD1 |
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| DOID:0110334 | osteogenesis imperfecta type 1 | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:0060230 | basal ganglia calcification | HGNC:8804 | Homo sapiens (human) | 5159 | PDGFRB |
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| DOID:0060369 | Parkinson's disease 6 | HGNC:14581 | Homo sapiens (human) | 65018 | PINK1 |
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| DOID:0110186 | Charcot-Marie-Tooth disease type 4D | HGNC:7679 | Homo sapiens (human) | 10397 | NDRG1 |
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| DOID:0050427 | xeroderma pigmentosum | HGNC:12816 | Homo sapiens (human) | 7508 | XPC |
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| DOID:0080598 | Kleefstra syndrome 2 | HGNC:13726 | Homo sapiens (human) | 58508 | KMT2C |
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| DOID:0050676 | Birt-Hogg-Dube syndrome | HGNC:27310 | Homo sapiens (human) | 201163 | FLCN |
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| DOID:2841 | asthma | HGNC:20823 | Homo sapiens (human) | 57628 | DPP10 |
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| DOID:0111103 | maturity-onset diabetes of the young type 4 | HGNC:6107 | Homo sapiens (human) | 3651 | PDX1 |
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| DOID:0060473 | Kabuki syndrome | HGNC:12637 | Homo sapiens (human) | 7403 | KDM6A |
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| DOID:0050464 | Farber lipogranulomatosis | HGNC:735 | Homo sapiens (human) | 427 | ASAH1 |
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| DOID:0110229 | cataract 6 multiple types | HGNC:3386 | Homo sapiens (human) | 1969 | EPHA2 |
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| DOID:13544 | low tension glaucoma | HGNC:17142 | Homo sapiens (human) | 10133 | OPTN |
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| DOID:9263 | homocystinuria | HGNC:1550 | Homo sapiens (human) | 875 | CBS |
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| DOID:1168 | familial hyperlipidemia | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
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| DOID:0050445 | X-linked dominant hypophosphatemic rickets | HGNC:8918 | Homo sapiens (human) | 5251 | PHEX |
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| DOID:0060887 | ossification of the posterior longitudinal ligament of spine | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
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| DOID:9970 | obesity | RGD:2289 | Rattus norvegicus (Norway rat) | 24889 | Cckar |
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| DOID:3209 | junctional epidermolysis bullosa | HGNC:6483 | Homo sapiens (human) | 3909 | LAMA3 |
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| DOID:1574 | alcohol use disorder | HGNC:2689 | Homo sapiens (human) | 1621 | DBH |
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| DOID:1339 | Diamond-Blackfan anemia | HGNC:26087 | Homo sapiens (human) | 55027 | HEATR3 |
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