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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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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:2355 | anemia | SGD:S000001949 | Saccharomyces cerevisiae S288C | 850614 | HXK1 |
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| DOID:4194 | glucose metabolism disease | SGD:S000001949 | Saccharomyces cerevisiae S288C | 850614 | HXK1 |
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| DOID:9952 | acute lymphoblastic leukemia | SGD:S000001949 | Saccharomyces cerevisiae S288C | 850614 | HXK1 |
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| DOID:9256 | colorectal cancer | SGD:S000001949 | Saccharomyces cerevisiae S288C | 850614 | HXK1 |
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| DOID:11054 | urinary bladder cancer | SGD:S000001949 | Saccharomyces cerevisiae S288C | 850614 | HXK1 |
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| DOID:12858 | Huntington's disease | SGD:S000001943 | Saccharomyces cerevisiae S288C | 850608 | BNA6 |
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| DOID:1287 | cardiovascular system disease | SGD:S000001911 | Saccharomyces cerevisiae S288C | 850569 | GSY1 |
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| DOID:3534 | Lafora disease | SGD:S000001911 | Saccharomyces cerevisiae S288C | 850569 | GSY1 |
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| DOID:2747 | glycogen storage disease | SGD:S000001911 | Saccharomyces cerevisiae S288C | 850569 | GSY1 |
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| DOID:4621 | holoprosencephaly | SGD:S000001869 | Saccharomyces cerevisiae S288C | 850519 | BST1 |
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| DOID:5154 | borna disease | HGNC:8605 | Homo sapiens (human) | 8505 | PARG |
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| DOID:3454 | brain infarction | HGNC:8605 | Homo sapiens (human) | 8505 | PARG |
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| DOID:0070352 | stress-induced childhood-onset neurodegeneration with variable ataxia and seizures | HGNC:8605 | Homo sapiens (human) | 8505 | PARG |
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| DOID:0050570 | congenital disorder of glycosylation type I | SGD:S000001849 | Saccharomyces cerevisiae S288C | 850499 | SEC53 |
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| DOID:5212 | congenital disorder of glycosylation | SGD:S000001849 | Saccharomyces cerevisiae S288C | 850499 | SEC53 |
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| DOID:0080552 | congenital disorder of glycosylation Ia | SGD:S000001849 | Saccharomyces cerevisiae S288C | 850499 | SEC53 |
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| DOID:583 | hemolytic anemia | SGD:S000000605 | Saccharomyces cerevisiae S288C | 850370 | PGK1 |
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| DOID:162 | cancer | SGD:S000000605 | Saccharomyces cerevisiae S288C | 850370 | PGK1 |
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| DOID:0111933 | phosphoglycerate kinase 1 deficiency | SGD:S000000605 | Saccharomyces cerevisiae S288C | 850370 | PGK1 |
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| DOID:14330 | Parkinson's disease | SGD:S000000605 | Saccharomyces cerevisiae S288C | 850370 | PGK1 |
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| DOID:7998 | hyperthyroidism | SGD:S000000598 | Saccharomyces cerevisiae S288C | 850361 | CIT2 |
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| DOID:0050852 | limb ischemia | SGD:S000000598 | Saccharomyces cerevisiae S288C | 850361 | CIT2 |
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| DOID:8466 | retinal degeneration | SGD:S000000598 | Saccharomyces cerevisiae S288C | 850361 | CIT2 |
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| DOID:1459 | hypothyroidism | SGD:S000000598 | Saccharomyces cerevisiae S288C | 850361 | CIT2 |
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| DOID:5844 | myocardial infarction | SGD:S000000598 | Saccharomyces cerevisiae S288C | 850361 | CIT2 |
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