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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
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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:11446 | sciatic neuropathy | HGNC:2590 | Homo sapiens (human) | 1583 | CYP11A1 |
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| DOID:0050811 | congenital adrenal hyperplasia | HGNC:2590 | Homo sapiens (human) | 1583 | CYP11A1 |
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| DOID:0080568 | congenital disorder of glycosylation Iq | HGNC:25812 | Homo sapiens (human) | 79644 | SRD5A3 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:25812 | Homo sapiens (human) | 79644 | SRD5A3 |
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| DOID:0050807 | Kahrizi syndrome | HGNC:25812 | Homo sapiens (human) | 79644 | SRD5A3 |
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| DOID:4621 | holoprosencephaly | HGNC:25712 | Homo sapiens (human) | 80055 | PGAP1 |
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| DOID:14330 | Parkinson's disease | HGNC:256 | Homo sapiens (human) | 131 | ADH7 |
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| DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | HGNC:25590 | Homo sapiens (human) | 55753 | OGDHL |
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| DOID:0081326 | oxoglutarate dehydrogenase deficiency | HGNC:25590 | Homo sapiens (human) | 55753 | OGDHL |
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| DOID:10907 | microcephaly | HGNC:25575 | Homo sapiens (human) | 55224 | ETNK2 |
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| DOID:10273 | heart conduction disease | HGNC:25575 | Homo sapiens (human) | 55224 | ETNK2 |
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| DOID:1826 | epilepsy | HGNC:25575 | Homo sapiens (human) | 55224 | ETNK2 |
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| DOID:987 | alopecia | HGNC:25531 | Homo sapiens (human) | 55711 | FAR2 |
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| DOID:10140 | dry eye syndrome | HGNC:25531 | Homo sapiens (human) | 55711 | FAR2 |
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| DOID:2841 | asthma | HGNC:253 | Homo sapiens (human) | 128 | ADH5 |
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| DOID:0080952 | AMED syndrome | HGNC:253 | Homo sapiens (human) | 128 | ADH5 |
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| DOID:1574 | alcohol use disorder | HGNC:253 | Homo sapiens (human) | 128 | ADH5 |
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| DOID:13580 | cholestasis | HGNC:253 | Homo sapiens (human) | 128 | ADH5 |
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| DOID:12798 | mucopolysaccharidosis | HGNC:25239 | Homo sapiens (human) | 153642 | ARSK |
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| DOID:1184 | nephrotic syndrome | HGNC:25223 | Homo sapiens (human) | 27235 | COQ2 |
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| DOID:0050730 | coenzyme Q10 deficiency disease | HGNC:25223 | Homo sapiens (human) | 27235 | COQ2 |
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| DOID:4752 | multiple system atrophy | HGNC:25223 | Homo sapiens (human) | 27235 | COQ2 |
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| DOID:0070238 | primary coenzyme Q10 deficiency 1 | HGNC:25223 | Homo sapiens (human) | 27235 | COQ2 |
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| DOID:10603 | glucose intolerance | HGNC:25223 | Homo sapiens (human) | 27235 | COQ2 |
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| DOID:0050741 | alcohol dependence | HGNC:252 | Homo sapiens (human) | 127 | ADH4 |
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