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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:9976 | heroin dependence | HGNC:4092 | Homo sapiens (human) | 2571 | GAD1 |
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| DOID:1826 | epilepsy | HGNC:4092 | Homo sapiens (human) | 2571 | GAD1 |
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| DOID:0050741 | alcohol dependence | HGNC:4092 | Homo sapiens (human) | 2571 | GAD1 |
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| DOID:2560 | morphine dependence | HGNC:4092 | Homo sapiens (human) | 2571 | GAD1 |
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| DOID:0060841 | isolated microphthalmia 8 | HGNC:409 | Homo sapiens (human) | 220 | ALDH1A3 |
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| DOID:1826 | epilepsy | HGNC:408 | Homo sapiens (human) | 7915 | ALDH5A1 |
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| DOID:0060175 | succinic semialdehyde dehydrogenase deficiency | HGNC:408 | Homo sapiens (human) | 7915 | ALDH5A1 |
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| DOID:9970 | obesity | HGNC:407 | Homo sapiens (human) | 219 | ALDH1B1 |
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| DOID:2752 | glycogen storage disease II | HGNC:4065 | Homo sapiens (human) | 2548 | GAA |
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| DOID:2749 | glycogen storage disease Ia | HGNC:4061 | Homo sapiens (human) | 2542 | SLC37A4 |
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| DOID:0081330 | glycogen storage disease Ib | HGNC:4061 | Homo sapiens (human) | 2542 | SLC37A4 |
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| DOID:0081331 | glycogen storage disease Ic | HGNC:4061 | Homo sapiens (human) | 2542 | SLC37A4 |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:4061 | Homo sapiens (human) | 2542 | SLC37A4 |
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| DOID:14067 | Plasmodium falciparum malaria | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:5844 | myocardial infarction | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:224 | transient cerebral ischemia | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:2383 | neonatal jaundice | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:557 | kidney disease | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:13413 | hepatic encephalopathy | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:1591 | renovascular hypertension | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:6713 | cerebrovascular disease | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:9281 | phenylketonuria | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:12365 | malaria | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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