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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:0111187 | distal myopathy with anterior tibial onset | MGI:1349385 | Mus musculus (house mouse) | 26903 | Dysf |
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| DOID:2581 | chondrodysplasia punctata | HGNC:3133 | Homo sapiens (human) | 10682 | EBP |
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| DOID:0080352 | X-linked chondrodysplasia punctata 2 | HGNC:3133 | Homo sapiens (human) | 10682 | EBP |
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| DOID:0111865 | MEND syndrome | HGNC:3133 | Homo sapiens (human) | 10682 | EBP |
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| DOID:0060292 | X-linked chondrodysplasia punctata 1 | HGNC:3133 | Homo sapiens (human) | 10682 | EBP |
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| DOID:1826 | epilepsy | SGD:S000004274 | Saccharomyces cerevisiae S288C | 850990 | ECI1 |
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| DOID:1485 | cystic fibrosis | HGNC:18967 | Homo sapiens (human) | 9695 | EDEM1 |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:16787 | Homo sapiens (human) | 80267 | EDEM3 |
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| DOID:0060668 | anencephaly | HGNC:3225 | Homo sapiens (human) | 1946 | EFNA5 |
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| DOID:0080759 | Fanconi renotubular syndrome 3 | HGNC:3247 | Homo sapiens (human) | 1962 | EHHADH |
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| DOID:10588 | adrenoleukodystrophy | HGNC:14418 | Homo sapiens (human) | 64834 | ELOVL1 |
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| DOID:2566 | corneal dystrophy | HGNC:14415 | Homo sapiens (human) | 6785 | ELOVL4 |
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| DOID:0050817 | Stargardt disease | HGNC:14415 | Homo sapiens (human) | 6785 | ELOVL4 |
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| DOID:0050981 | spinocerebellar ataxia type 34 | HGNC:14415 | Homo sapiens (human) | 6785 | ELOVL4 |
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| DOID:0050985 | spinocerebellar ataxia type 38 | HGNC:21308 | Homo sapiens (human) | 60481 | ELOVL5 |
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| DOID:10588 | adrenoleukodystrophy | HGNC:26292 | Homo sapiens (human) | 79993 | ELOVL7 |
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| DOID:9993 | hypoglycemia | SGD:S000002924 | Saccharomyces cerevisiae S288C | 852128 | EMI2 |
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| DOID:0070216 | familial hyperinsulinemic hypoglycemia 3 | SGD:S000002924 | Saccharomyces cerevisiae S288C | 852128 | EMI2 |
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| DOID:11714 | gestational diabetes | SGD:S000002924 | Saccharomyces cerevisiae S288C | 852128 | EMI2 |
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| DOID:9351 | diabetes mellitus | SGD:S000002924 | Saccharomyces cerevisiae S288C | 852128 | EMI2 |
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| DOID:0111100 | maturity-onset diabetes of the young type 2 | SGD:S000002924 | Saccharomyces cerevisiae S288C | 852128 | EMI2 |
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| DOID:3393 | coronary artery disease | SGD:S000002924 | Saccharomyces cerevisiae S288C | 852128 | EMI2 |
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| DOID:10763 | hypertension | SGD:S000002924 | Saccharomyces cerevisiae S288C | 852128 | EMI2 |
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| DOID:9352 | type 2 diabetes mellitus | SGD:S000002924 | Saccharomyces cerevisiae S288C | 852128 | EMI2 |
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| DOID:13317 | hyperinsulinemic hypoglycemia | SGD:S000002924 | Saccharomyces cerevisiae S288C | 852128 | EMI2 |
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