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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:0111671 | primary hyperoxaluria type 2 | HGNC:4570 | Homo sapiens (human) | 9380 | GRHPR |
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| DOID:341 | peripheral vascular disease | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:13550 | angle-closure glaucoma | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:0080855 | Parkinsonism | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:10652 | Alzheimer's disease | HGNC:24864 | Homo sapiens (human) | 26330 | GAPDHS |
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| DOID:7998 | hyperthyroidism | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:5844 | myocardial infarction | HGNC:15917 | Homo sapiens (human) | 23236 | PLCB1 |
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| DOID:824 | periodontitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:5041 | esophageal cancer | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:4367 | apparent mineralocorticoid excess syndrome | HGNC:5209 | Homo sapiens (human) | 3291 | HSD11B2 |
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| DOID:8805 | intermediate coronary syndrome | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:653 | purine-pyrimidine metabolic disorder | HGNC:12563 | Homo sapiens (human) | 7372 | UMPS |
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| DOID:0112216 | developmental and epileptic encephalopathy 80 | HGNC:8959 | Homo sapiens (human) | 9488 | PIGB |
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| DOID:1205 | allergic disease | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0110210 | Charcot-Marie-Tooth disease X-linked recessive 5 | HGNC:9462 | Homo sapiens (human) | 5631 | PRPS1 |
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| DOID:3650 | lactic acidosis | HGNC:9725 | Homo sapiens (human) | 5836 | PYGL |
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| DOID:0050811 | congenital adrenal hyperplasia | HGNC:2593 | Homo sapiens (human) | 1586 | CYP17A1 |
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| DOID:326 | ischemia | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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| DOID:0080388 | nephrotic syndrome type 7 | HGNC:2852 | Homo sapiens (human) | 8526 | DGKE |
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| DOID:0060041 | autism spectrum disorder | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:8947 | diabetic retinopathy | HGNC:4323 | Homo sapiens (human) | 2739 | GLO1 |
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| DOID:1485 | cystic fibrosis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:4440 | seminoma | HGNC:3148 | Homo sapiens (human) | 1890 | TYMP |
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| DOID:1927 | sphingolipidosis | HGNC:735 | Homo sapiens (human) | 427 | ASAH1 |
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| DOID:1485 | cystic fibrosis | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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