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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:0080547 | metabolic dysfunction-associated steatohepatitis | SGD:S000006008 | Saccharomyces cerevisiae S288C | 856018 | YDC1 |
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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:0060284 | paroxysmal nocturnal hemoglobinuria | SGD:S000006096 | Saccharomyces cerevisiae S288C | 855928 | SPT14 |
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| DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | SGD:S000006096 | Saccharomyces cerevisiae S288C | 855928 | SPT14 |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | SGD:S000006096 | Saccharomyces cerevisiae S288C | 855928 | SPT14 |
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| DOID:0080322 | polycystic kidney disease | SGD:S000006148 | Saccharomyces cerevisiae S288C | 855874 | ALG5 |
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| DOID:0050570 | congenital disorder of glycosylation type I | SGD:S000006148 | Saccharomyces cerevisiae S288C | 855874 | ALG5 |
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| DOID:0080855 | Parkinsonism | SGD:S000006202 | Saccharomyces cerevisiae S288C | 855848 | ERR2 |
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| DOID:14115 | toxic shock syndrome | SGD:S000006202 | Saccharomyces cerevisiae S288C | 855848 | ERR2 |
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| DOID:10763 | hypertension | SGD:S000006202 | Saccharomyces cerevisiae S288C | 855848 | ERR2 |
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| DOID:11832 | visual epilepsy | SGD:S000006202 | Saccharomyces cerevisiae S288C | 855848 | ERR2 |
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| DOID:1712 | aortic valve stenosis | SGD:S000006202 | Saccharomyces cerevisiae S288C | 855848 | ERR2 |
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| DOID:10652 | Alzheimer's disease | SGD:S000006202 | Saccharomyces cerevisiae S288C | 855848 | ERR2 |
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| DOID:9870 | galactosemia | SGD:S000005354 | Saccharomyces cerevisiae S288C | 855808 | YNR071C |
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| DOID:0050570 | congenital disorder of glycosylation type I | SGD:S000005313 | Saccharomyces cerevisiae S288C | 855764 | ALG12 |
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| DOID:0080559 | congenital disorder of glycosylation Ig | SGD:S000005313 | Saccharomyces cerevisiae S288C | 855764 | ALG12 |
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| DOID:0050852 | limb ischemia | SGD:S000005284 | Saccharomyces cerevisiae S288C | 855732 | CIT1 |
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| DOID:5844 | myocardial infarction | SGD:S000005284 | Saccharomyces cerevisiae S288C | 855732 | CIT1 |
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| DOID:7998 | hyperthyroidism | SGD:S000005284 | Saccharomyces cerevisiae S288C | 855732 | CIT1 |
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| DOID:1459 | hypothyroidism | SGD:S000005284 | Saccharomyces cerevisiae S288C | 855732 | CIT1 |
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| DOID:12930 | dilated cardiomyopathy | SGD:S000005284 | Saccharomyces cerevisiae S288C | 855732 | CIT1 |
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| DOID:8466 | retinal degeneration | SGD:S000005284 | Saccharomyces cerevisiae S288C | 855732 | CIT1 |
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