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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:4852 | pleomorphic xanthoastrocytoma | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:2986 | IgA glomerulonephritis | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:3770 | pulmonary fibrosis | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:11396 | pulmonary edema | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:114 | heart disease | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:2747 | glycogen storage disease | HGNC:4699 | Homo sapiens (human) | 2992 | GYG1 |
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| DOID:162 | cancer | HGNC:8896 | Homo sapiens (human) | 5230 | PGK1 |
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| DOID:9268 | glycine encephalopathy | HGNC:4208 | Homo sapiens (human) | 2653 | GCSH |
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| DOID:0080552 | congenital disorder of glycosylation Ia | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:4450 | renal cell carcinoma | HGNC:8729 | Homo sapiens (human) | 5111 | PCNA |
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| DOID:11335 | sarcoidosis | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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| DOID:10024 | migraine with aura | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:0112223 | developmental and epileptic encephalopathy 89 | HGNC:4092 | Homo sapiens (human) | 2571 | GAD1 |
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| DOID:0110184 | Charcot-Marie-Tooth disease type 4J | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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| DOID:0060576 | 3MC syndrome 2 | HGNC:17213 | Homo sapiens (human) | 78989 | COLEC11 |
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| DOID:2957 | pulmonary tuberculosis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:783 | end stage renal disease | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:2367 | neuroaxonal dystrophy | HGNC:9039 | Homo sapiens (human) | 8398 | PLA2G6 |
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| DOID:10211 | cholelithiasis | HGNC:2593 | Homo sapiens (human) | 1586 | CYP17A1 |
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| DOID:784 | chronic kidney disease | HGNC:9922 | Homo sapiens (human) | 5950 | RBP4 |
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| DOID:3649 | pyruvate decarboxylase deficiency | HGNC:2896 | Homo sapiens (human) | 1737 | DLAT |
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| DOID:0080178 | mucositis | HGNC:8729 | Homo sapiens (human) | 5111 | PCNA |
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| DOID:2316 | brain ischemia | HGNC:8729 | Homo sapiens (human) | 5111 | PCNA |
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| DOID:3525 | middle cerebral artery infarction | HGNC:6783 | Homo sapiens (human) | 4099 | MAG |
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| DOID:2228 | thrombocytosis | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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