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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: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: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:4621 | holoprosencephaly | SGD:S000001869 | Saccharomyces cerevisiae S288C | 850519 | BST1 |
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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:12858 | Huntington's disease | SGD:S000001943 | Saccharomyces cerevisiae S288C | 850608 | BNA6 |
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| DOID:0110196 | Charcot-Marie-Tooth disease type 4G | SGD:S000001949 | Saccharomyces cerevisiae S288C | 850614 | HXK1 |
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| DOID:9452 | steatotic liver disease | SGD:S000001949 | Saccharomyces cerevisiae S288C | 850614 | HXK1 |
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| DOID:10923 | sickle cell anemia | SGD:S000001949 | Saccharomyces cerevisiae S288C | 850614 | HXK1 |
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| DOID:3393 | coronary artery disease | SGD:S000001949 | Saccharomyces cerevisiae S288C | 850614 | HXK1 |
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| DOID:6432 | pulmonary hypertension | SGD:S000001949 | Saccharomyces cerevisiae S288C | 850614 | HXK1 |
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| DOID:9970 | obesity | SGD:S000001949 | Saccharomyces cerevisiae S288C | 850614 | HXK1 |
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| DOID:11714 | gestational diabetes | SGD:S000001949 | Saccharomyces cerevisiae S288C | 850614 | HXK1 |
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| DOID:2861 | congenital nonspherocytic hemolytic anemia | SGD:S000001949 | Saccharomyces cerevisiae S288C | 850614 | HXK1 |
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| DOID:9351 | diabetes mellitus | SGD:S000001949 | Saccharomyces cerevisiae S288C | 850614 | HXK1 |
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| DOID:0111100 | maturity-onset diabetes of the young type 2 | SGD:S000001949 | Saccharomyces cerevisiae S288C | 850614 | HXK1 |
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| DOID:0060639 | permanent neonatal diabetes mellitus | SGD:S000001949 | Saccharomyces cerevisiae S288C | 850614 | HXK1 |
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| DOID:9993 | hypoglycemia | SGD:S000001949 | Saccharomyces cerevisiae S288C | 850614 | HXK1 |
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| DOID:9352 | type 2 diabetes mellitus | SGD:S000001949 | Saccharomyces cerevisiae S288C | 850614 | HXK1 |
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| DOID:10763 | hypertension | SGD:S000001949 | Saccharomyces cerevisiae S288C | 850614 | HXK1 |
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