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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:0080056 | achondrogenesis type II | Xenbase:XB-GENE-6252613 | Xenopus laevis (African clawed frog) | 397738 | col2a1.L |
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| DOID:0080055 | achondrogenesis type IB | RGD:620622 | Rattus norvegicus (Norway rat) | 117267 | Slc26a2 |
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| DOID:0080055 | achondrogenesis type IB | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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| DOID:0080055 | achondrogenesis type IB | MGI:892977 | Mus musculus (house mouse) | 13521 | Slc26a2 |
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| DOID:0080054 | achondrogenesis type IA | HGNC:12305 | Homo sapiens (human) | 9321 | TRIP11 |
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| DOID:0080053 | Albright's hereditary osteodystrophy | HGNC:4392 | Homo sapiens (human) | 2778 | GNAS |
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| DOID:0080053 | Albright's hereditary osteodystrophy | MGI:95777 | Mus musculus (house mouse) | 14683 | Gnas |
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| DOID:0080053 | Albright's hereditary osteodystrophy | HGNC:9607 | Homo sapiens (human) | 5744 | PTHLH |
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| DOID:0080052 | acromesomelic dysplasia, Grebe type | HGNC:4220 | Homo sapiens (human) | 8200 | GDF5 |
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| DOID:0080052 | acromesomelic dysplasia, Grebe type | MGI:95688 | Mus musculus (house mouse) | 14563 | Gdf5 |
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| DOID:0080051 | acromesomelic dysplasia, Hunter-Thompson type | HGNC:4220 | Homo sapiens (human) | 8200 | GDF5 |
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| DOID:0080051 | acromesomelic dysplasia, Hunter-Thompson type | MGI:95688 | Mus musculus (house mouse) | 14563 | Gdf5 |
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| DOID:0080050 | acromesomelic dysplasia, Maroteaux type | HGNC:7944 | Homo sapiens (human) | 4882 | NPR2 |
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| DOID:0080050 | acromesomelic dysplasia, Maroteaux type | MGI:97372 | Mus musculus (house mouse) | 230103 | Npr2 |
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| DOID:0080050 | acromesomelic dysplasia, Maroteaux type | WB:WBGene00020131 | Caenorhabditis elegans | 172051 | gcy-28 |
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| DOID:0080050 | acromesomelic dysplasia, Maroteaux type | RGD:620851 | Rattus norvegicus (Norway rat) | 116564 | Npr2 |
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| DOID:0080047 | pseudoachondroplasia | MGI:88469 | Mus musculus (house mouse) | 12845 | Comp |
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| DOID:0080047 | pseudoachondroplasia | RGD:2378 | Rattus norvegicus (Norway rat) | 25304 | Comp |
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| DOID:0080047 | pseudoachondroplasia | HGNC:2227 | Homo sapiens (human) | 1311 | COMP |
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| DOID:0080047 | pseudoachondroplasia | FB:FBgn0031850 | Drosophila melanogaster (fruit fly) | 33941 | Tsp | CG11326 |
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| DOID:0080046 | Stickler syndrome | MGI:88452 | Mus musculus (house mouse) | 12824 | Col2a1 |
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| DOID:0080046 | Stickler syndrome | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:0080046 | Stickler syndrome | Xenbase:XB-GENE-6258353 | Xenopus tropicalis (tropical clawed frog) | 394828 | col2a1 |
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| DOID:0080046 | Stickler syndrome | HGNC:2186 | Homo sapiens (human) | 1301 | COL11A1 |
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| DOID:0080046 | Stickler syndrome | RGD:2375 | Rattus norvegicus (Norway rat) | 25412 | Col2a1 |
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