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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:0070259 | congenital disorder of glycosylation type IIg | HGNC:6545 | Homo sapiens (human) | 9382 | COG1 |
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| DOID:3070 | high grade glioma | HGNC:2172 | Homo sapiens (human) | 6900 | CNTN2 |
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| DOID:850 | lung disease | HGNC:2172 | Homo sapiens (human) | 6900 | CNTN2 |
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| DOID:0111691 | familial adult myoclonic epilepsy 5 | HGNC:2172 | Homo sapiens (human) | 6900 | CNTN2 |
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| DOID:0080101 | Compton-North congenital myopathy | HGNC:2171 | Homo sapiens (human) | 1272 | CNTN1 |
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| DOID:1312 | focal segmental glomerulosclerosis | HGNC:18290 | Homo sapiens (human) | 55907 | CMAS |
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| DOID:0110728 | neuronal ceroid lipofuscinosis 5 | HGNC:2076 | Homo sapiens (human) | 1203 | CLN5 |
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| DOID:13564 | aspergillosis | HGNC:14558 | Homo sapiens (human) | 64581 | CLEC7A |
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| DOID:2058 | chronic mucocutaneous candidiasis | HGNC:14558 | Homo sapiens (human) | 64581 | CLEC7A |
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| DOID:13564 | aspergillosis | HGNC:24355 | Homo sapiens (human) | 51267 | CLEC1A |
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| DOID:2377 | multiple sclerosis | HGNC:29013 | Homo sapiens (human) | 23274 | CLEC16A |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:29013 | Homo sapiens (human) | 23274 | CLEC16A |
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| DOID:13774 | Addison's disease | HGNC:29013 | Homo sapiens (human) | 23274 | CLEC16A |
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| DOID:7148 | rheumatoid arthritis | HGNC:29013 | Homo sapiens (human) | 23274 | CLEC16A |
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| DOID:1289 | neurodegenerative disease | HGNC:29013 | Homo sapiens (human) | 23274 | CLEC16A |
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| DOID:7998 | hyperthyroidism | SGD:S000006205 | Saccharomyces cerevisiae S288C | 856107 | CIT3 |
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| DOID:3312 | bipolar disorder | SGD:S000006205 | Saccharomyces cerevisiae S288C | 856107 | CIT3 |
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| DOID:12930 | dilated cardiomyopathy | SGD:S000006205 | Saccharomyces cerevisiae S288C | 856107 | CIT3 |
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| DOID:5844 | myocardial infarction | SGD:S000006205 | Saccharomyces cerevisiae S288C | 856107 | CIT3 |
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| DOID:8466 | retinal degeneration | SGD:S000006205 | Saccharomyces cerevisiae S288C | 856107 | CIT3 |
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| DOID:6000 | congestive heart failure | SGD:S000006205 | Saccharomyces cerevisiae S288C | 856107 | CIT3 |
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| DOID:1459 | hypothyroidism | SGD:S000006205 | Saccharomyces cerevisiae S288C | 856107 | CIT3 |
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| DOID:11984 | hypertrophic cardiomyopathy | SGD:S000006205 | Saccharomyces cerevisiae S288C | 856107 | CIT3 |
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| DOID:0050852 | limb ischemia | SGD:S000006205 | Saccharomyces cerevisiae S288C | 856107 | CIT3 |
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| DOID:7998 | hyperthyroidism | SGD:S000000598 | Saccharomyces cerevisiae S288C | 850361 | CIT2 |
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