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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:0060475 | myoclonic-atonic epilepsy | MGI:1353497 | Mus musculus (house mouse) | 27376 | Slc25a10 |
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| DOID:0070329 | mitochondrial DNA depletion syndrome | MGI:1353497 | Mus musculus (house mouse) | 27376 | Slc25a10 |
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| DOID:0070450 | mitochondrial DNA depletion syndrome 19 | MGI:1353497 | Mus musculus (house mouse) | 27376 | Slc25a10 |
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| DOID:0060536 | mitochondrial complex I deficiency | MGI:1353497 | Mus musculus (house mouse) | 27376 | Slc25a10 |
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| DOID:2747 | glycogen storage disease | MGI:1351614 | Mus musculus (house mouse) | 27357 | Gyg1 |
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| DOID:0050579 | glycogen storage disease XV | MGI:1351614 | Mus musculus (house mouse) | 27357 | Gyg1 |
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| DOID:5723 | optic atrophy | HGNC:29622 | Homo sapiens (human) | 27349 | MCAT |
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| DOID:1574 | alcohol use disorder | HGNC:491 | Homo sapiens (human) | 27329 | ANGPTL3 |
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| DOID:0111061 | familial hypobetalipoproteinemia 2 | HGNC:491 | Homo sapiens (human) | 27329 | ANGPTL3 |
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| DOID:0070435 | hyperphosphatasia with impaired intellectual development syndrome 3 | HGNC:17893 | Homo sapiens (human) | 27315 | PGAP2 |
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| DOID:9268 | glycine encephalopathy | HGNC:4313 | Homo sapiens (human) | 2731 | GLDC |
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| DOID:10534 | stomach cancer | HGNC:4313 | Homo sapiens (human) | 2731 | GLDC |
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| DOID:5082 | liver cirrhosis | HGNC:4311 | Homo sapiens (human) | 2729 | GCLC |
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| DOID:5844 | myocardial infarction | HGNC:4311 | Homo sapiens (human) | 2729 | GCLC |
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| DOID:1485 | cystic fibrosis | HGNC:4311 | Homo sapiens (human) | 2729 | GCLC |
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| DOID:9256 | colorectal cancer | HGNC:4311 | Homo sapiens (human) | 2729 | GCLC |
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| DOID:83 | cataract | HGNC:4311 | Homo sapiens (human) | 2729 | GCLC |
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| DOID:0111681 | glutamate-cysteine ligase deficiency | HGNC:4311 | Homo sapiens (human) | 2729 | GCLC |
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| DOID:9675 | pulmonary emphysema | HGNC:4311 | Homo sapiens (human) | 2729 | GCLC |
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| DOID:583 | hemolytic anemia | HGNC:4311 | Homo sapiens (human) | 2729 | GCLC |
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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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