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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:2349 | arteriosclerosis | HGNC:438 | Homo sapiens (human) | 249 | ALPL |
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| DOID:0110913 | adult hypophosphatasia | HGNC:438 | Homo sapiens (human) | 249 | ALPL |
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| DOID:9452 | steatotic liver disease | HGNC:438 | Homo sapiens (human) | 249 | ALPL |
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| DOID:14213 | hypophosphatasia | HGNC:438 | Homo sapiens (human) | 249 | ALPL |
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| DOID:11054 | urinary bladder cancer | HGNC:451 | Homo sapiens (human) | 23600 | AMACR |
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| DOID:3459 | breast carcinoma | HGNC:451 | Homo sapiens (human) | 23600 | AMACR |
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| DOID:0060602 | alpha-methylacyl-CoA racemase deficiency | HGNC:451 | Homo sapiens (human) | 23600 | AMACR |
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| DOID:8634 | prostate carcinoma in situ | HGNC:451 | Homo sapiens (human) | 23600 | AMACR |
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| DOID:0111068 | congenital bile acid synthesis defect 4 | HGNC:451 | Homo sapiens (human) | 23600 | AMACR |
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| DOID:4450 | renal cell carcinoma | HGNC:451 | Homo sapiens (human) | 23600 | AMACR |
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| DOID:9268 | glycine encephalopathy | HGNC:473 | Homo sapiens (human) | 275 | AMT |
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| DOID:1574 | alcohol use disorder | HGNC:491 | Homo sapiens (human) | 27329 | ANGPTL3 |
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| DOID:0111061 | familial hypobetalipoproteinemia 2 | HGNC:491 | Homo sapiens (human) | 27329 | ANGPTL3 |
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| DOID:10873 | Kuhnt-Junius degeneration | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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| DOID:2921 | glomerulonephritis | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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| DOID:14330 | Parkinson's disease | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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| DOID:1459 | hypothyroidism | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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| DOID:11383 | cryptorchidism | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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| DOID:893 | Wilson disease | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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| DOID:10652 | Alzheimer's disease | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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| DOID:438 | autoimmune disease of the nervous system | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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| DOID:418 | systemic scleroderma | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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| DOID:7998 | hyperthyroidism | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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| DOID:0080379 | nephrotic syndrome type 2 | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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| DOID:5844 | myocardial infarction | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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