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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: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:0110942 | autosomal recessive osteopetrosis 1 | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
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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:0110915 | childhood 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:0110913 | adult hypophosphatasia | HGNC:438 | Homo sapiens (human) | 249 | ALPL |
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| DOID:0110870 | congenital stationary night blindness 1A | HGNC:8082 | Homo sapiens (human) | 60506 | NYX |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | RGD:620916 | Rattus norvegicus (Norway rat) | 170911 | Pik3ca |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:20575 | Homo sapiens (human) | 284541 | CYP4A22 |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:2642 | Homo sapiens (human) | 1579 | CYP4A11 |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:9008 | Homo sapiens (human) | 5310 | PKD1 |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | RGD:2081 | Rattus norvegicus (Norway rat) | 24185 | Akt1 |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | MGI:87986 | Mus musculus (house mouse) | 11651 | Akt1 |
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| 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:0110860 | polycystic kidney disease 3 | MGI:1097667 | Mus musculus (house mouse) | 14376 | Ganab |
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