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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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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MIRAGE
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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol ▼ | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:12236 | primary biliary cholangitis | HGNC:21747 | Homo sapiens (human) | 80315 | CPEB4 |
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| DOID:10762 | portal hypertension | HGNC:21747 | Homo sapiens (human) | 80315 | CPEB4 |
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| DOID:5082 | liver cirrhosis | HGNC:21747 | Homo sapiens (human) | 80315 | CPEB4 |
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| DOID:10762 | portal hypertension | HGNC:21744 | Homo sapiens (human) | 64506 | CPEB1 |
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| DOID:5082 | liver cirrhosis | HGNC:21744 | Homo sapiens (human) | 64506 | CPEB1 |
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| DOID:3068 | glioblastoma | HGNC:21744 | Homo sapiens (human) | 64506 | CPEB1 |
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| DOID:12236 | primary biliary cholangitis | HGNC:21744 | Homo sapiens (human) | 64506 | CPEB1 |
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| DOID:9452 | steatotic liver disease | HGNC:2303 | Homo sapiens (human) | 1363 | CPE |
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| DOID:0050741 | alcohol dependence | HGNC:2303 | Homo sapiens (human) | 1363 | CPE |
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| DOID:9970 | obesity | HGNC:2303 | Homo sapiens (human) | 1363 | CPE |
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| DOID:3393 | coronary artery disease | HGNC:2303 | Homo sapiens (human) | 1363 | CPE |
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| DOID:3068 | glioblastoma | HGNC:2303 | Homo sapiens (human) | 1363 | CPE |
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| DOID:1936 | atherosclerosis | HGNC:2303 | Homo sapiens (human) | 1363 | CPE |
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| DOID:11981 | morbid obesity | HGNC:2303 | Homo sapiens (human) | 1363 | CPE |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:2303 | Homo sapiens (human) | 1363 | CPE |
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| DOID:13241 | Behcet's disease | HGNC:2300 | Homo sapiens (human) | 1361 | CPB2 |
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| DOID:9970 | obesity | HGNC:2300 | Homo sapiens (human) | 1361 | CPB2 |
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| DOID:9351 | diabetes mellitus | HGNC:2300 | Homo sapiens (human) | 1361 | CPB2 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:2300 | Homo sapiens (human) | 1361 | CPB2 |
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| DOID:1184 | nephrotic syndrome | HGNC:2300 | Homo sapiens (human) | 1361 | CPB2 |
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| DOID:2228 | thrombocytosis | HGNC:2300 | Homo sapiens (human) | 1361 | CPB2 |
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| DOID:784 | chronic kidney disease | HGNC:2300 | Homo sapiens (human) | 1361 | CPB2 |
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| DOID:0111308 | familial febrile seizures 11 | HGNC:17245 | Homo sapiens (human) | 57094 | CPA6 |
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| DOID:0060752 | familial temporal lobe epilepsy 5 | HGNC:17245 | Homo sapiens (human) | 57094 | CPA6 |
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| DOID:7998 | hyperthyroidism | HGNC:2295 | Homo sapiens (human) | 1356 | CP |
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