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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:0070256 | congenital disorder of glycosylation type IId | RGD:620900 | Rattus norvegicus (Norway rat) | 24390 | B4galt1 |
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| DOID:0110777 | hereditary spastic paraplegia 26 | MGI:1342057 | Mus musculus (house mouse) | 14421 | B4galnt1 |
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| DOID:0110777 | hereditary spastic paraplegia 26 | RGD:620490 | Rattus norvegicus (Norway rat) | 64828 | B4galnt1 |
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| DOID:0050560 | Walker-Warburg syndrome | HGNC:15685 | Homo sapiens (human) | 11041 | B4GAT1 |
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| DOID:0111238 | congenital muscular dystrophy-dystroglycanopathy type A13 | HGNC:15685 | Homo sapiens (human) | 11041 | B4GAT1 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | HGNC:15685 | Homo sapiens (human) | 11041 | B4GAT1 |
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| DOID:0080738 | Ehlers-Danlos syndrome spondylodysplastic type 1 | HGNC:930 | Homo sapiens (human) | 11285 | B4GALT7 |
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| DOID:13359 | Ehlers-Danlos syndrome | HGNC:930 | Homo sapiens (human) | 11285 | B4GALT7 |
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| DOID:2377 | multiple sclerosis | HGNC:929 | Homo sapiens (human) | 9331 | B4GALT6 |
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| DOID:2377 | multiple sclerosis | HGNC:928 | Homo sapiens (human) | 9334 | B4GALT5 |
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| DOID:2986 | IgA glomerulonephritis | HGNC:924 | Homo sapiens (human) | 2683 | B4GALT1 |
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| DOID:0070256 | congenital disorder of glycosylation type IId | HGNC:924 | Homo sapiens (human) | 2683 | B4GALT1 |
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| DOID:5212 | congenital disorder of glycosylation | HGNC:924 | Homo sapiens (human) | 2683 | B4GALT1 |
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| DOID:28 | endocrine system disease | HGNC:924 | Homo sapiens (human) | 2683 | B4GALT1 |
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| DOID:0110777 | hereditary spastic paraplegia 26 | HGNC:4117 | Homo sapiens (human) | 2583 | B4GALNT1 |
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| DOID:0080201 | Peters plus syndrome | RGD:1588723 | Rattus norvegicus (Norway rat) | 689765 | B3glct |
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| DOID:0080201 | Peters plus syndrome | MGI:2685903 | Mus musculus (house mouse) | 381694 | B3glct |
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| DOID:0080575 | Larsen-like syndrome B3GAT3 type | MGI:1919977 | Mus musculus (house mouse) | 72727 | B3gat3 |
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| DOID:0080575 | Larsen-like syndrome B3GAT3 type | RGD:1311968 | Rattus norvegicus (Norway rat) | 293722 | B3gat3 |
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| DOID:5419 | schizophrenia | RGD:620903 | Rattus norvegicus (Norway rat) | 64544 | B3gat2 |
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| DOID:5419 | schizophrenia | MGI:2389490 | Mus musculus (house mouse) | 280645 | B3gat2 |
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| DOID:9206 | Barrett's esophagus | RGD:620903 | Rattus norvegicus (Norway rat) | 64544 | B3gat2 |
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| DOID:9206 | Barrett's esophagus | MGI:2389490 | Mus musculus (house mouse) | 280645 | B3gat2 |
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| DOID:3770 | pulmonary fibrosis | RGD:70880 | Rattus norvegicus (Norway rat) | 117108 | B3gat1 |
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| DOID:3770 | pulmonary fibrosis | MGI:1924148 | Mus musculus (house mouse) | 76898 | B3gat1 |
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