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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:10588 | adrenoleukodystrophy | HGNC:26292 | Homo sapiens (human) | 79993 | ELOVL7 |
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| DOID:0050985 | spinocerebellar ataxia type 38 | HGNC:21308 | Homo sapiens (human) | 60481 | ELOVL5 |
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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:10588 | adrenoleukodystrophy | HGNC:14418 | Homo sapiens (human) | 64834 | ELOVL1 |
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| DOID:0080759 | Fanconi renotubular syndrome 3 | HGNC:3247 | Homo sapiens (human) | 1962 | EHHADH |
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| DOID:0060668 | anencephaly | HGNC:3225 | Homo sapiens (human) | 1946 | EFNA5 |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:16787 | Homo sapiens (human) | 80267 | EDEM3 |
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| DOID:1485 | cystic fibrosis | HGNC:18967 | Homo sapiens (human) | 9695 | EDEM1 |
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| DOID:1826 | epilepsy | SGD:S000004274 | Saccharomyces cerevisiae S288C | 850990 | ECI1 |
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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:0070199 | Miyoshi muscular dystrophy 1 | MGI:1349385 | Mus musculus (house mouse) | 26903 | Dysf |
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| DOID:11724 | limb-girdle muscular dystrophy | MGI:1349385 | Mus musculus (house mouse) | 26903 | Dysf |
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| DOID:11720 | distal myopathy | MGI:1349385 | Mus musculus (house mouse) | 26903 | Dysf |
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| DOID:0110276 | autosomal recessive limb-girdle muscular dystrophy type 2B | MGI:1349385 | Mus musculus (house mouse) | 26903 | Dysf |
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| DOID:9884 | muscular dystrophy | MGI:1349385 | Mus musculus (house mouse) | 26903 | Dysf |
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| DOID:0111187 | distal myopathy with anterior tibial onset | MGI:1349385 | Mus musculus (house mouse) | 26903 | Dysf |
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| DOID:0111156 | spermatogenic failure 9 | RGD:1564311 | Rattus norvegicus (Norway rat) | 300461 | Dpy19l2 |
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| DOID:0111156 | spermatogenic failure 9 | MGI:2444662 | Mus musculus (house mouse) | 320752 | Dpy19l2 |
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| DOID:0112376 | muscular dystrophy-dystroglycanopathy type B15 | FB:FBgn0053977 | Drosophila melanogaster (fruit fly) | 3885575 | Dpm3 | CG33977 |
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| DOID:0050570 | congenital disorder of glycosylation type I | FB:FBgn0053977 | Drosophila melanogaster (fruit fly) | 3885575 | Dpm3 | CG33977 |
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