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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:0111040 | glycogen storage disease IXd | WB:WBGene00015754 | Caenorhabditis elegans | 176149 | C14B9.8 |
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| DOID:0111040 | glycogen storage disease IXd | MGI:97576 | Mus musculus (house mouse) | 18679 | Phka1 |
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| DOID:0111040 | glycogen storage disease IXd | HGNC:8925 | Homo sapiens (human) | 5255 | PHKA1 |
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| DOID:0111037 | glycine N-methyltransferase deficiency | HGNC:4415 | Homo sapiens (human) | 27232 | GNMT |
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| DOID:0111037 | glycine N-methyltransferase deficiency | MGI:1202304 | Mus musculus (house mouse) | 14711 | Gnmt |
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| DOID:0111037 | glycine N-methyltransferase deficiency | RGD:2719 | Rattus norvegicus (Norway rat) | 25134 | Gnmt |
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| DOID:0111035 | CADASIL 1 | FB:FBgn0004647 | Drosophila melanogaster (fruit fly) | 31293 | N | CG3936 |
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| DOID:0111027 | hemochromatosis type 2A | HGNC:4887 | Homo sapiens (human) | 148738 | HJV |
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| DOID:0110980 | Joubert syndrome 1 | FB:FBgn0036273 | Drosophila melanogaster (fruit fly) | 39404 | INPP5E |
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| DOID:0110980 | Joubert syndrome 1 | HGNC:21474 | Homo sapiens (human) | 56623 | INPP5E |
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| DOID:0110961 | atypical Gaucher's disease due to saposin c deficiency | HGNC:9498 | Homo sapiens (human) | 5660 | PSAP |
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| DOID:0110960 | Gaucher's disease perinatal lethal | WB:WBGene00021160 | Caenorhabditis elegans | 177314 | gba-4 |
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| DOID:0110960 | Gaucher's disease perinatal lethal | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:0110960 | Gaucher's disease perinatal lethal | MGI:95665 | Mus musculus (house mouse) | 14466 | Gba1 |
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| DOID:0110960 | Gaucher's disease perinatal lethal | WB:WBGene00008706 | Caenorhabditis elegans | 178535 | gba-3 |
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| DOID:0110959 | Gaucher's disease type III | MGI:95665 | Mus musculus (house mouse) | 14466 | Gba1 |
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| DOID:0110959 | Gaucher's disease type III | WB:WBGene00008706 | Caenorhabditis elegans | 178535 | gba-3 |
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| DOID:0110959 | Gaucher's disease type III | WB:WBGene00021160 | Caenorhabditis elegans | 177314 | gba-4 |
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| DOID:0110959 | Gaucher's disease type III | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:0110958 | Gaucher's disease type II | MGI:95665 | Mus musculus (house mouse) | 14466 | Gba1 |
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| DOID:0110958 | Gaucher's disease type II | WB:WBGene00016340 | Caenorhabditis elegans | 183155 | gba-2 |
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| DOID:0110958 | Gaucher's disease type II | WB:WBGene00021160 | Caenorhabditis elegans | 177314 | gba-4 |
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| DOID:0110958 | Gaucher's disease type II | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:0110958 | Gaucher's disease type II | WB:WBGene00008706 | Caenorhabditis elegans | 178535 | gba-3 |
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| DOID:0110958 | Gaucher's disease type II | WB:WBGene00016335 | Caenorhabditis elegans | 173574 | gba-1 |
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