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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:9409 | diabetes insipidus | HGNC:4819 | Homo sapiens (human) | 3037 | HAS2 |
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| DOID:6432 | pulmonary hypertension | HGNC:4819 | Homo sapiens (human) | 3037 | HAS2 |
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| DOID:6432 | pulmonary hypertension | HGNC:4818 | Homo sapiens (human) | 3036 | HAS1 |
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| DOID:9452 | steatotic liver disease | HGNC:4803 | Homo sapiens (human) | 3032 | HADHB |
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| DOID:10652 | Alzheimer's disease | HGNC:4803 | Homo sapiens (human) | 3032 | HADHB |
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| DOID:3146 | lipid metabolism disorder | HGNC:4803 | Homo sapiens (human) | 3032 | HADHB |
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| DOID:0111277 | mitochondrial trifunctional protein deficiency | HGNC:4803 | Homo sapiens (human) | 3032 | HADHB |
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| DOID:700 | mitochondrial metabolism disease | HGNC:4803 | Homo sapiens (human) | 3032 | HADHB |
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| DOID:9452 | steatotic liver disease | HGNC:4801 | Homo sapiens (human) | 3030 | HADHA |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:4801 | Homo sapiens (human) | 3030 | HADHA |
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| DOID:0111277 | mitochondrial trifunctional protein deficiency | HGNC:4801 | Homo sapiens (human) | 3030 | HADHA |
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| DOID:3146 | lipid metabolism disorder | HGNC:4801 | Homo sapiens (human) | 3030 | HADHA |
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| DOID:10652 | Alzheimer's disease | HGNC:4801 | Homo sapiens (human) | 3030 | HADHA |
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| DOID:5844 | myocardial infarction | HGNC:4799 | Homo sapiens (human) | 3033 | HADH |
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| DOID:0070215 | familial hyperinsulinemic hypoglycemia 4 | HGNC:4799 | Homo sapiens (human) | 3033 | HADH |
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| DOID:9970 | obesity | HGNC:4799 | Homo sapiens (human) | 3033 | HADH |
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| DOID:0090141 | cortisone reductase deficiency 1 | HGNC:4795 | Homo sapiens (human) | 9563 | H6PD |
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| DOID:2377 | multiple sclerosis | HGNC:4795 | Homo sapiens (human) | 9563 | H6PD |
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| DOID:0090139 | cortisone reductase deficiency | HGNC:4795 | Homo sapiens (human) | 9563 | H6PD |
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| DOID:9268 | glycine encephalopathy | HGNC:473 | Homo sapiens (human) | 275 | AMT |
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| DOID:3534 | Lafora disease | HGNC:4707 | Homo sapiens (human) | 2998 | GYS2 |
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| DOID:2747 | glycogen storage disease | HGNC:4707 | Homo sapiens (human) | 2998 | GYS2 |
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| DOID:3534 | Lafora disease | HGNC:4706 | Homo sapiens (human) | 2997 | GYS1 |
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| DOID:1287 | cardiovascular system disease | HGNC:4706 | Homo sapiens (human) | 2997 | GYS1 |
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| DOID:2747 | glycogen storage disease | HGNC:4699 | Homo sapiens (human) | 2992 | GYG1 |
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