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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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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 | July 29, 2024 |
| Disease ID ▲ | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | MGI:1206581 | Mus musculus (house mouse) | 18706 | Pik3ca |
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| DOID:0110870 | congenital stationary night blindness 1A | HGNC:8082 | Homo sapiens (human) | 60506 | NYX |
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| DOID:0110913 | adult hypophosphatasia | HGNC:438 | Homo sapiens (human) | 249 | ALPL |
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| DOID:0110914 | infantile hypophosphatasia | HGNC:438 | Homo sapiens (human) | 249 | ALPL |
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| DOID:0110915 | childhood hypophosphatasia | HGNC:438 | Homo sapiens (human) | 249 | ALPL |
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| DOID:0110937 | autosomal dominant osteopetrosis 1 | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:0110937 | autosomal dominant osteopetrosis 1 | MGI:1278315 | Mus musculus (house mouse) | 16973 | Lrp5 |
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| DOID:0110942 | autosomal recessive osteopetrosis 1 | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
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| DOID:0110957 | Gaucher's disease type I | MGI:95665 | Mus musculus (house mouse) | 14466 | Gba1 |
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| DOID:0110957 | Gaucher's disease type I | WB:WBGene00021160 | Caenorhabditis elegans | 177314 | gba-4 |
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| DOID:0110957 | Gaucher's disease type I | WB:WBGene00008706 | Caenorhabditis elegans | 178535 | gba-3 |
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| DOID:0110957 | Gaucher's disease type I | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:0110957 | Gaucher's disease type I | WB:WBGene00016335 | Caenorhabditis elegans | 173574 | gba-1 |
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| DOID:0110957 | Gaucher's disease type I | WB:WBGene00016340 | Caenorhabditis elegans | 183155 | gba-2 |
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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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| 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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