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GlyTouCan
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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID ▲ | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:3209 | junctional epidermolysis bullosa | WB:WBGene00002247 | Caenorhabditis elegans | 177292 | lam-1 |
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| DOID:0110054 | amelogenesis imperfecta type 1A | WB:WBGene00002247 | Caenorhabditis elegans | 177292 | lam-1 |
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| DOID:0080380 | nephrotic syndrome type 5 | WB:WBGene00002247 | Caenorhabditis elegans | 177292 | lam-1 |
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| DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | WB:WBGene00002248 | Caenorhabditis elegans | 172952 | lam-3 |
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| DOID:1591 | renovascular hypertension | WB:WBGene00002248 | Caenorhabditis elegans | 172952 | lam-3 |
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| DOID:11830 | myopia | WB:WBGene00002248 | Caenorhabditis elegans | 172952 | lam-3 |
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| DOID:0110636 | congenital merosin-deficient muscular dystrophy 1A | WB:WBGene00002248 | Caenorhabditis elegans | 172952 | lam-3 |
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| DOID:9884 | muscular dystrophy | WB:WBGene00002248 | Caenorhabditis elegans | 172952 | lam-3 |
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| DOID:10983 | Alport syndrome | WB:WBGene00002280 | Caenorhabditis elegans | 181708 | let-2 |
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| DOID:0111547 | retinal arterial tortuosity | WB:WBGene00002280 | Caenorhabditis elegans | 181708 | let-2 |
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| DOID:0110034 | X-linked Alport syndrome | WB:WBGene00002280 | Caenorhabditis elegans | 181708 | let-2 |
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| DOID:557 | kidney disease | WB:WBGene00002280 | Caenorhabditis elegans | 181708 | let-2 |
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| DOID:0050560 | Walker-Warburg syndrome | WB:WBGene00002280 | Caenorhabditis elegans | 181708 | let-2 |
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| DOID:854 | collagen disease | WB:WBGene00002280 | Caenorhabditis elegans | 181708 | let-2 |
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| DOID:0110033 | autosomal recessive Alport syndrome | WB:WBGene00002280 | Caenorhabditis elegans | 181708 | let-2 |
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| DOID:0111740 | X-linked deafness 6 | WB:WBGene00002280 | Caenorhabditis elegans | 181708 | let-2 |
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| DOID:0090125 | brain small vessel disease 1 | WB:WBGene00002280 | Caenorhabditis elegans | 181708 | let-2 |
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| DOID:423 | myopathy | WB:WBGene00002280 | Caenorhabditis elegans | 181708 | let-2 |
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| DOID:5844 | myocardial infarction | WB:WBGene00002280 | Caenorhabditis elegans | 181708 | let-2 |
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| DOID:0060263 | porencephaly | WB:WBGene00002280 | Caenorhabditis elegans | 181708 | let-2 |
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| DOID:9970 | obesity | WB:WBGene00002280 | Caenorhabditis elegans | 181708 | let-2 |
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| DOID:13223 | uterine fibroid | WB:WBGene00002280 | Caenorhabditis elegans | 181708 | let-2 |
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| DOID:6432 | pulmonary hypertension | WB:WBGene00002280 | Caenorhabditis elegans | 181708 | let-2 |
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| DOID:576 | proteinuria | WB:WBGene00002280 | Caenorhabditis elegans | 181708 | let-2 |
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| DOID:2671 | transitional cell carcinoma | WB:WBGene00002299 | Caenorhabditis elegans | 174462 | let-23 |
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