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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:10588 | adrenoleukodystrophy | HGNC:29567 | Homo sapiens (human) | 23205 | ACSBG1 |
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| DOID:0111067 | congenital bile acid synthesis defect 6 | HGNC:120 | Homo sapiens (human) | 8309 | ACOX2 |
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| DOID:9970 | obesity | FB:FBgn0027572 | Drosophila melanogaster (fruit fly) | 37028 | ACOX1 |
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| DOID:9452 | steatotic liver disease | FB:FBgn0027572 | Drosophila melanogaster (fruit fly) | 37028 | ACOX1 |
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| DOID:0070516 | Mitchell syndrome | FB:FBgn0027572 | Drosophila melanogaster (fruit fly) | 37028 | ACOX1 |
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| DOID:0050797 | peroxisomal acyl-CoA oxidase deficiency | HGNC:119 | Homo sapiens (human) | 51 | ACOX1 |
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| DOID:9452 | steatotic liver disease | HGNC:119 | Homo sapiens (human) | 51 | ACOX1 |
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| DOID:906 | peroxisomal disease | FB:FBgn0027572 | Drosophila melanogaster (fruit fly) | 37028 | ACOX1 |
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| DOID:9970 | obesity | HGNC:119 | Homo sapiens (human) | 51 | ACOX1 |
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| DOID:906 | peroxisomal disease | HGNC:119 | Homo sapiens (human) | 51 | ACOX1 |
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| DOID:0070516 | Mitchell syndrome | HGNC:119 | Homo sapiens (human) | 51 | ACOX1 |
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| DOID:0050797 | peroxisomal acyl-CoA oxidase deficiency | FB:FBgn0027572 | Drosophila melanogaster (fruit fly) | 37028 | ACOX1 |
|
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| DOID:9352 | type 2 diabetes mellitus | HGNC:18431 | Homo sapiens (human) | 10965 | ACOT2 |
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| DOID:3571 | liver cancer | HGNC:24436 | Homo sapiens (human) | 134526 | ACOT12 |
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| DOID:331 | central nervous system disease | HGNC:118 | Homo sapiens (human) | 50 | ACO2 |
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| DOID:0111442 | optic atrophy 9 | HGNC:118 | Homo sapiens (human) | 50 | ACO2 |
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| DOID:14330 | Parkinson's disease | HGNC:118 | Homo sapiens (human) | 50 | ACO2 |
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| DOID:1289 | neurodegenerative disease | HGNC:118 | Homo sapiens (human) | 50 | ACO2 |
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| DOID:0050883 | infantile cerebellar-retinal degeneration | HGNC:118 | Homo sapiens (human) | 50 | ACO2 |
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| DOID:1891 | optic nerve disease | HGNC:118 | Homo sapiens (human) | 50 | ACO2 |
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| DOID:331 | central nervous system disease | SGD:S000004295 | Saccharomyces cerevisiae S288C | 851013 | ACO1 |
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| DOID:13268 | porphyria | HGNC:117 | Homo sapiens (human) | 48 | ACO1 |
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| DOID:14330 | Parkinson's disease | SGD:S000004295 | Saccharomyces cerevisiae S288C | 851013 | ACO1 |
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| DOID:1289 | neurodegenerative disease | SGD:S000004295 | Saccharomyces cerevisiae S288C | 851013 | ACO1 |
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| DOID:0111442 | optic atrophy 9 | SGD:S000004295 | Saccharomyces cerevisiae S288C | 851013 | ACO1 |
|
