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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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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:2754 | glycogen storage disease VI | HGNC:9725 | Homo sapiens (human) | 5836 | PYGL |
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| DOID:0080507 | Cornelia de Lange syndrome 3 | HGNC:2468 | Homo sapiens (human) | 9126 | SMC3 |
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| DOID:0050644 | arterial calcification of infancy | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
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| DOID:4795 | GM2 gangliosidosis, AB variant | HGNC:4367 | Homo sapiens (human) | 2760 | GM2A |
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| DOID:12365 | malaria | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:4450 | renal cell carcinoma | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:3770 | pulmonary fibrosis | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:0050545 | visceral heterotaxy | HGNC:18292 | Homo sapiens (human) | 55997 | CFC1 |
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| DOID:0050770 | polycystic liver disease | HGNC:9411 | Homo sapiens (human) | 5589 | PRKCSH |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:417 | Homo sapiens (human) | 229 | ALDOB |
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| DOID:0060563 | Char syndrome | HGNC:11743 | Homo sapiens (human) | 7021 | TFAP2B |
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| DOID:0060350 | adenine phosphoribosyltransferase deficiency | HGNC:626 | Homo sapiens (human) | 353 | APRT |
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| DOID:10763 | hypertension | HGNC:3402 | Homo sapiens (human) | 2053 | EPHX2 |
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| DOID:11211 | buphthalmos | HGNC:2597 | Homo sapiens (human) | 1545 | CYP1B1 |
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| DOID:0090005 | Schwartz-Jampel syndrome 1 | HGNC:5273 | Homo sapiens (human) | 3339 | HSPG2 |
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| DOID:0110852 | rhizomelic chondrodysplasia punctata type 2 | HGNC:4416 | Homo sapiens (human) | 8443 | GNPAT |
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| DOID:0080633 | developmental cardiac valvular defect | HGNC:9067 | Homo sapiens (human) | 5337 | PLD1 |
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| DOID:2747 | glycogen storage disease | RGD:620024 | Rattus norvegicus (Norway rat) | 140671 | Phkg2 |
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| DOID:0111237 | congenital muscular dystrophy-dystroglycanopathy type A1 | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:0111040 | glycogen storage disease IXd | HGNC:8925 | Homo sapiens (human) | 5255 | PHKA1 |
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| DOID:0080349 | developmental and epileptic encephalopathy 39 | HGNC:10982 | Homo sapiens (human) | 8604 | SLC25A12 |
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| DOID:684 | hepatocellular carcinoma | RGD:3369 | Rattus norvegicus (Norway rat) | 25747 | Ppara |
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| DOID:9884 | muscular dystrophy | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:1064 | cystinosis | HGNC:2518 | Homo sapiens (human) | 1497 | CTNS |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:9291 | Homo sapiens (human) | 5506 | PPP1R3A |
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