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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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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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:1936 | atherosclerosis | HGNC:9922 | Homo sapiens (human) | 5950 | RBP4 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:9922 | Homo sapiens (human) | 5950 | RBP4 |
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| DOID:5844 | myocardial infarction | HGNC:9952 | Homo sapiens (human) | 5968 | REG1B |
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| DOID:219 | colon cancer | HGNC:9952 | Homo sapiens (human) | 5968 | REG1B |
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| DOID:11446 | sciatic neuropathy | HGNC:29595 | Homo sapiens (human) | 130120 | REG3G |
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| DOID:11832 | visual epilepsy | HGNC:29595 | Homo sapiens (human) | 130120 | REG3G |
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| DOID:552 | pneumonia | HGNC:29595 | Homo sapiens (human) | 130120 | REG3G |
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| DOID:2913 | acute pancreatitis | HGNC:29595 | Homo sapiens (human) | 130120 | REG3G |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:29595 | Homo sapiens (human) | 130120 | REG3G |
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| DOID:0080566 | congenital disorder of glycosylation In | SGD:S000000116 | Saccharomyces cerevisiae S288C | 852261 | RFT1 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:30220 | Homo sapiens (human) | 91869 | RFT1 |
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| DOID:0050570 | congenital disorder of glycosylation type I | SGD:S000000116 | Saccharomyces cerevisiae S288C | 852261 | RFT1 |
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| DOID:162 | cancer | SGD:S000000116 | Saccharomyces cerevisiae S288C | 852261 | RFT1 |
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| DOID:162 | cancer | HGNC:30220 | Homo sapiens (human) | 91869 | RFT1 |
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| DOID:0080566 | congenital disorder of glycosylation In | HGNC:30220 | Homo sapiens (human) | 91869 | RFT1 |
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| DOID:2377 | multiple sclerosis | HGNC:30308 | Homo sapiens (human) | 56963 | RGMA |
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| DOID:3328 | temporal lobe epilepsy | HGNC:30308 | Homo sapiens (human) | 56963 | RGMA |
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| DOID:11446 | sciatic neuropathy | HGNC:30308 | Homo sapiens (human) | 56963 | RGMA |
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| DOID:3525 | middle cerebral artery infarction | HGNC:30308 | Homo sapiens (human) | 56963 | RGMA |
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| DOID:1168 | familial hyperlipidemia | HGNC:9989 | Homo sapiens (human) | 9104 | RGN |
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| DOID:684 | hepatocellular carcinoma | HGNC:9989 | Homo sapiens (human) | 9104 | RGN |
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| DOID:10534 | stomach cancer | HGNC:9989 | Homo sapiens (human) | 9104 | RGN |
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| DOID:9408 | acute myocardial infarction | SGD:S000006369 | Saccharomyces cerevisiae S288C | 856294 | RHO1 |
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| DOID:4001 | ovarian carcinoma | SGD:S000006369 | Saccharomyces cerevisiae S288C | 856294 | RHO1 |
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| DOID:1289 | neurodegenerative disease | SGD:S000006369 | Saccharomyces cerevisiae S288C | 856294 | RHO1 |
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