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GlyTouCan
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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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID ▼ | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0060173 | Timothy syndrome | HGNC:1391 | Homo sapiens (human) | 776 | CACNA1D |
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| DOID:5419 | schizophrenia | HGNC:1391 | Homo sapiens (human) | 776 | CACNA1D |
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| DOID:5426 | primary ovarian insufficiency | HGNC:13909 | Homo sapiens (human) | 58524 | DMRT3 |
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| DOID:10952 | nephritis | HGNC:13902 | Homo sapiens (human) | 8710 | SERPINB7 |
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| DOID:2986 | IgA glomerulonephritis | HGNC:13902 | Homo sapiens (human) | 8710 | SERPINB7 |
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| DOID:0050831 | familial encephalopathy with neuroserpin inclusion bodies | HGNC:13902 | Homo sapiens (human) | 8710 | SERPINB7 |
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| DOID:0110649 | long QT syndrome 8 | HGNC:1390 | Homo sapiens (human) | 775 | CACNA1C |
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| DOID:0070536 | neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures | HGNC:1390 | Homo sapiens (human) | 775 | CACNA1C |
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| DOID:0050741 | alcohol dependence | HGNC:1390 | Homo sapiens (human) | 775 | CACNA1C |
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| DOID:0060173 | Timothy syndrome | HGNC:1390 | Homo sapiens (human) | 775 | CACNA1C |
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| DOID:11723 | Duchenne muscular dystrophy | HGNC:1390 | Homo sapiens (human) | 775 | CACNA1C |
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| DOID:0110220 | Brugada syndrome 3 | HGNC:1390 | Homo sapiens (human) | 775 | CACNA1C |
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| DOID:0050214 | Lambert-Eaton myasthenic syndrome | HGNC:1389 | Homo sapiens (human) | 774 | CACNA1B |
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| DOID:1826 | epilepsy | HGNC:1389 | Homo sapiens (human) | 774 | CACNA1B |
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| DOID:6364 | migraine | HGNC:1389 | Homo sapiens (human) | 774 | CACNA1B |
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| DOID:0111181 | familial hemiplegic migraine 1 | HGNC:1389 | Homo sapiens (human) | 774 | CACNA1B |
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| DOID:2377 | multiple sclerosis | HGNC:1389 | Homo sapiens (human) | 774 | CACNA1B |
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| DOID:0050951 | hereditary ataxia | HGNC:1389 | Homo sapiens (human) | 774 | CACNA1B |
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| DOID:4724 | brain edema | HGNC:1389 | Homo sapiens (human) | 774 | CACNA1B |
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| DOID:13580 | cholestasis | HGNC:13887 | Homo sapiens (human) | 64241 | ABCG8 |
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| DOID:1168 | familial hyperlipidemia | HGNC:13887 | Homo sapiens (human) | 64241 | ABCG8 |
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| DOID:2349 | arteriosclerosis | HGNC:13887 | Homo sapiens (human) | 64241 | ABCG8 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:13887 | Homo sapiens (human) | 64241 | ABCG8 |
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| DOID:9970 | obesity | HGNC:13887 | Homo sapiens (human) | 64241 | ABCG8 |
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| DOID:0090019 | sitosterolemia | HGNC:13887 | Homo sapiens (human) | 64241 | ABCG8 |
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