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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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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:2355 | anemia | WB:WBGene00009920 | Caenorhabditis elegans | 172613 | abts-1 |
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| DOID:4947 | cholangiocarcinoma | WB:WBGene00009920 | Caenorhabditis elegans | 172613 | abts-1 |
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| DOID:0110839 | Usher syndrome type 2C | WB:WBGene00009920 | Caenorhabditis elegans | 172613 | abts-1 |
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| DOID:5212 | congenital disorder of glycosylation | WB:WBGene00009925 | Caenorhabditis elegans | 178364 | F52B11.2 |
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| DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00009925 | Caenorhabditis elegans | 178364 | F52B11.2 |
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| DOID:0080552 | congenital disorder of glycosylation Ia | WB:WBGene00009925 | Caenorhabditis elegans | 178364 | F52B11.2 |
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| DOID:0060717 | autosomal recessive congenital ichthyosis 8 | WB:WBGene00010062 | Caenorhabditis elegans | 179771 | lipl-1 |
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| DOID:14497 | Wolman disease | WB:WBGene00010062 | Caenorhabditis elegans | 179771 | lipl-1 |
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| DOID:0080217 | lysosomal acid lipase deficiency | WB:WBGene00010062 | Caenorhabditis elegans | 179771 | lipl-1 |
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| DOID:14502 | cholesterol ester storage disease | WB:WBGene00010062 | Caenorhabditis elegans | 179771 | lipl-1 |
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| DOID:10825 | essential hypertension | WB:WBGene00010117 | Caenorhabditis elegans | 181494 | nkb-3 |
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| DOID:9970 | obesity | WB:WBGene00010117 | Caenorhabditis elegans | 181494 | nkb-3 |
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| DOID:10003 | sensorineural hearing loss | WB:WBGene00010117 | Caenorhabditis elegans | 181494 | nkb-3 |
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| DOID:1826 | epilepsy | WB:WBGene00010117 | Caenorhabditis elegans | 181494 | nkb-3 |
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| DOID:9074 | systemic lupus erythematosus | WB:WBGene00010284 | Caenorhabditis elegans | 179632 | aman-2 |
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| DOID:5419 | schizophrenia | WB:WBGene00010284 | Caenorhabditis elegans | 179632 | aman-2 |
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| DOID:1338 | congenital dyserythropoietic anemia | WB:WBGene00010284 | Caenorhabditis elegans | 179632 | aman-2 |
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| DOID:10609 | rickets | WB:WBGene00010356 | Caenorhabditis elegans | 181616 | famk-1 |
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| DOID:2187 | amelogenesis imperfecta | WB:WBGene00010356 | Caenorhabditis elegans | 181616 | famk-1 |
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| DOID:0110066 | amelogenesis imperfecta type 1G | WB:WBGene00010356 | Caenorhabditis elegans | 181616 | famk-1 |
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| DOID:0050445 | X-linked dominant hypophosphatemic rickets | WB:WBGene00010356 | Caenorhabditis elegans | 181616 | famk-1 |
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| DOID:0060227 | Adams-Oliver syndrome | WB:WBGene00010386 | Caenorhabditis elegans | 179990 | H12D21.10 |
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| DOID:1612 | breast cancer | WB:WBGene00010537 | Caenorhabditis elegans | 173281 | mys-2 |
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| DOID:4467 | clear cell renal cell carcinoma | WB:WBGene00010537 | Caenorhabditis elegans | 173281 | mys-2 |
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| DOID:0111238 | congenital muscular dystrophy-dystroglycanopathy type A13 | WB:WBGene00010694 | Caenorhabditis elegans | 3565692 | bgnt-1.5 |
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