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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:3905 | lung carcinoma | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0060071 | pre-malignant neoplasm | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:10787 | premature menopause | HGNC:94 | Homo sapiens (human) | 39 | ACAT2 |
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| DOID:3393 | coronary artery disease | HGNC:94 | Homo sapiens (human) | 39 | ACAT2 |
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| DOID:9970 | obesity | HGNC:93 | Homo sapiens (human) | 38 | ACAT1 |
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| DOID:2978 | carbohydrate metabolic disorder | HGNC:93 | Homo sapiens (human) | 38 | ACAT1 |
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| DOID:14723 | beta-ketothiolase deficiency | HGNC:93 | Homo sapiens (human) | 38 | ACAT1 |
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| DOID:2349 | arteriosclerosis | HGNC:93 | Homo sapiens (human) | 38 | ACAT1 |
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| DOID:783 | end stage renal disease | HGNC:93 | Homo sapiens (human) | 38 | ACAT1 |
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| DOID:1184 | nephrotic syndrome | HGNC:93 | Homo sapiens (human) | 38 | ACAT1 |
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| DOID:8398 | osteoarthritis | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
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| DOID:2377 | multiple sclerosis | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
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| DOID:6000 | congestive heart failure | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
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| DOID:1824 | status epilepticus | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
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| DOID:90 | degenerative disc disease | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
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| DOID:4480 | achondroplasia | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
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| DOID:7148 | rheumatoid arthritis | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
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| DOID:0112282 | spondyloepiphyseal dysplasia Kimberley type | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
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| DOID:10652 | Alzheimer's disease | HGNC:92 | Homo sapiens (human) | 37 | ACADVL |
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| DOID:0080155 | very long chain acyl-CoA dehydrogenase deficiency | HGNC:92 | Homo sapiens (human) | 37 | ACADVL |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:92 | Homo sapiens (human) | 37 | ACADVL |
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| DOID:1574 | alcohol use disorder | HGNC:90 | Homo sapiens (human) | 35 | ACADS |
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| DOID:0080154 | short chain acyl-CoA dehydrogenase deficiency | HGNC:90 | Homo sapiens (human) | 35 | ACADS |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:89 | Homo sapiens (human) | 34 | ACADM |
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| DOID:0080153 | medium chain acyl-CoA dehydrogenase deficiency | HGNC:89 | Homo sapiens (human) | 34 | ACADM |
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