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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:0080208 | metabolic dysfunction-associated steatotic liver disease | SGD:S000005771 | Saccharomyces cerevisiae S288C | 854419 | DGA1 |
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| DOID:9970 | obesity | HGNC:20113 | Homo sapiens (human) | 123099 | DEGS2 |
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| DOID:1289 | neurodegenerative disease | HGNC:20113 | Homo sapiens (human) | 123099 | DEGS2 |
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| DOID:0070399 | hypomyelinating leukodystrophy 18 | HGNC:13709 | Homo sapiens (human) | 8560 | DEGS1 |
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| DOID:9970 | obesity | HGNC:13709 | Homo sapiens (human) | 8560 | DEGS1 |
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| DOID:1289 | neurodegenerative disease | HGNC:13709 | Homo sapiens (human) | 8560 | DEGS1 |
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| DOID:0060786 | hypomyelinating leukodystrophy | HGNC:13709 | Homo sapiens (human) | 8560 | DEGS1 |
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| DOID:0080569 | congenital disorder of glycosylation Ir | HGNC:2728 | Homo sapiens (human) | 1650 | DDOST |
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| DOID:0111258 | pentosuria | HGNC:18985 | Homo sapiens (human) | 51181 | DCXR |
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| DOID:5844 | myocardial infarction | HGNC:2705 | Homo sapiens (human) | 1634 | DCN |
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| DOID:0060445 | congenital stromal corneal dystrophy | HGNC:2705 | Homo sapiens (human) | 1634 | DCN |
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| DOID:13359 | Ehlers-Danlos syndrome | HGNC:2705 | Homo sapiens (human) | 1634 | DCN |
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| DOID:3459 | breast carcinoma | HGNC:2705 | Homo sapiens (human) | 1634 | DCN |
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| DOID:9970 | obesity | HGNC:2705 | Homo sapiens (human) | 1634 | DCN |
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| DOID:3070 | high grade glioma | HGNC:2705 | Homo sapiens (human) | 1634 | DCN |
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| DOID:2841 | asthma | HGNC:2705 | Homo sapiens (human) | 1634 | DCN |
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| DOID:11714 | gestational diabetes | HGNC:2705 | Homo sapiens (human) | 1634 | DCN |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:2705 | Homo sapiens (human) | 1634 | DCN |
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| DOID:9269 | maple syrup urine disease | HGNC:2698 | Homo sapiens (human) | 1629 | DBT |
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| DOID:0111232 | congenital muscular dystrophy-dystroglycanopathy type A9 | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:0050453 | lissencephaly | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:11723 | Duchenne muscular dystrophy | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:12236 | primary biliary cholangitis | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:0050559 | Fukuyama congenital muscular dystrophy | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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