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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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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:0060696 | hyperekplexia 1 | HGNC:4326 | Homo sapiens (human) | 2741 | GLRA1 |
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| DOID:0060695 | hyperekplexia | ZFIN:ZDB-GENE-991117-1 | Danio rerio (zebrafish) | 30676 | glra1 |
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| DOID:0060695 | hyperekplexia | WB:WBGene00001592 | Caenorhabditis elegans | 172103 | glc-2 |
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| DOID:0060695 | hyperekplexia | RGD:2704 | Rattus norvegicus (Norway rat) | 25674 | Glra1 |
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| DOID:0060695 | hyperekplexia | MGI:95747 | Mus musculus (house mouse) | 14654 | Glra1 |
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| DOID:0060695 | hyperekplexia | WB:WBGene00001591 | Caenorhabditis elegans | 180086 | glc-1 |
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| DOID:0060695 | hyperekplexia | HGNC:4326 | Homo sapiens (human) | 2741 | GLRA1 |
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| DOID:0060693 | Brunner Syndrome | HGNC:6833 | Homo sapiens (human) | 4128 | MAOA |
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| DOID:0060692 | platelet-type bleeding disorder 8 | RGD:621681 | Rattus norvegicus (Norway rat) | 64803 | P2ry12 |
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| DOID:0060692 | platelet-type bleeding disorder 8 | HGNC:18124 | Homo sapiens (human) | 64805 | P2RY12 |
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| DOID:0060692 | platelet-type bleeding disorder 8 | MGI:1918089 | Mus musculus (house mouse) | 70839 | P2ry12 |
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| DOID:0060691 | platelet-type bleeding disorder 16 | WB:WBGene00003930 | Caenorhabditis elegans | 175504 | pat-3 |
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| DOID:0060691 | platelet-type bleeding disorder 16 | FB:FBgn0001250 | Drosophila melanogaster (fruit fly) | 32661 | if |
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| DOID:0060691 | platelet-type bleeding disorder 16 | MGI:96612 | Mus musculus (house mouse) | 16416 | Itgb3 |
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| DOID:0060691 | platelet-type bleeding disorder 16 | HGNC:6138 | Homo sapiens (human) | 3674 | ITGA2B |
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| DOID:0060691 | platelet-type bleeding disorder 16 | WB:WBGene00003929 | Caenorhabditis elegans | 176240 | pat-2 |
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| DOID:0060691 | platelet-type bleeding disorder 16 | RGD:628868 | Rattus norvegicus (Norway rat) | 29302 | Itgb3 |
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| DOID:0060691 | platelet-type bleeding disorder 16 | MGI:96601 | Mus musculus (house mouse) | 16399 | Itga2b |
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| DOID:0060691 | platelet-type bleeding disorder 16 | HGNC:6156 | Homo sapiens (human) | 3690 | ITGB3 |
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| DOID:0060691 | platelet-type bleeding disorder 16 | FB:FBgn0004657 | Drosophila melanogaster (fruit fly) | 44885 | mys |
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| DOID:0060690 | autosomal dominant auditory neuropathy 1 | SGD:S000005215 | Saccharomyces cerevisiae S288C | 855450 | BNI1 |
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| DOID:0060690 | autosomal dominant auditory neuropathy 1 | HGNC:2876 | Homo sapiens (human) | 1729 | DIAPH1 |
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| DOID:0060690 | autosomal dominant auditory neuropathy 1 | HGNC:15480 | Homo sapiens (human) | 81624 | DIAPH3 |
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| DOID:0060688 | arteriovenous malformations of the brain | RGD:2029 | Rattus norvegicus (Norway rat) | 25237 | Acvrl1 |
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| DOID:0060688 | arteriovenous malformations of the brain | WB:WBGene00004860 | Caenorhabditis elegans | 174044 | sma-6 |
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