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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: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: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: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:6432 | pulmonary hypertension | HGNC:4818 | Homo sapiens (human) | 3036 | HAS1 |
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| DOID:3525 | middle cerebral artery infarction | HGNC:4819 | Homo sapiens (human) | 3037 | HAS2 |
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| 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:4820 | Homo sapiens (human) | 3038 | HAS3 |
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| DOID:3320 | Tay-Sachs disease | HGNC:4878 | Homo sapiens (human) | 3073 | HEXA |
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| DOID:3323 | Sandhoff disease | HGNC:4879 | Homo sapiens (human) | 3074 | HEXB |
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| DOID:12377 | spinal muscular atrophy | HGNC:4879 | Homo sapiens (human) | 3074 | HEXB |
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| DOID:3211 | lysosomal storage disease | HGNC:4879 | Homo sapiens (human) | 3074 | HEXB |
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| DOID:0111027 | hemochromatosis type 2A | HGNC:4887 | Homo sapiens (human) | 148738 | HJV |
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| DOID:2352 | hemochromatosis | HGNC:4887 | Homo sapiens (human) | 148738 | HJV |
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| DOID:1574 | alcohol use disorder | HGNC:491 | Homo sapiens (human) | 27329 | ANGPTL3 |
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