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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:988 | mitral valve prolapse | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:4922 | Homo sapiens (human) | 3098 | HK1 |
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| DOID:1852 | intrahepatic cholestasis | HGNC:18324 | Homo sapiens (human) | 80270 | HSD3B7 |
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| DOID:0090139 | cortisone reductase deficiency | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:6432 | pulmonary hypertension | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:11335 | sarcoidosis | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:10720 | Homo sapiens (human) | 6402 | SELL |
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| DOID:4607 | biliary tract cancer | HGNC:9235 | Homo sapiens (human) | 5467 | PPARD |
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| DOID:11151 | cholecystolithiasis | HGNC:9031 | Homo sapiens (human) | 5320 | PLA2G2A |
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| DOID:0050156 | idiopathic pulmonary fibrosis | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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| DOID:11725 | Cornelia de Lange syndrome | HGNC:2468 | Homo sapiens (human) | 9126 | SMC3 |
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| DOID:1070 | primary open angle glaucoma | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:2861 | congenital nonspherocytic hemolytic anemia | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:10763 | hypertension | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
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| DOID:4810 | cerebrotendinous xanthomatosis | HGNC:2605 | Homo sapiens (human) | 1593 | CYP27A1 |
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| DOID:1324 | lung cancer | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:0112376 | muscular dystrophy-dystroglycanopathy type B15 | HGNC:3007 | Homo sapiens (human) | 54344 | DPM3 |
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| DOID:684 | hepatocellular carcinoma | HGNC:2468 | Homo sapiens (human) | 9126 | SMC3 |
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| DOID:3827 | congenital diaphragmatic hernia | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:0050328 | congenital hypothyroidism | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:11984 | hypertrophic cardiomyopathy | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:809 | cocaine abuse | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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| DOID:4543 | retrograde amnesia | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | HGNC:2651 | Homo sapiens (human) | 1581 | CYP7A1 |
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| DOID:3827 | congenital diaphragmatic hernia | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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