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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:0110296 | autosomal recessive limb-girdle muscular dystrophy type 2M | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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| DOID:9884 | muscular dystrophy | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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| DOID:0110284 | autosomal recessive limb-girdle muscular dystrophy type 2L | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
|
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| DOID:0110444 | dilated cardiomyopathy 1X | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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| DOID:0112379 | muscular dystrophy-dystroglycanopathy type B4 | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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| DOID:0050560 | Walker-Warburg syndrome | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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| DOID:0070433 | hyperphosphatasia with impaired intellectual development syndrome 1 | WB:WBGene00020375 | Caenorhabditis elegans | 172305 | pigv-1 |
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| DOID:0080573 | congenital disorder of glycosylation Ix | WB:WBGene00020437 | Caenorhabditis elegans | 175886 | stt-3 |
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| DOID:0080572 | congenital disorder of glycosylation Iw | WB:WBGene00020437 | Caenorhabditis elegans | 175886 | stt-3 |
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| DOID:3211 | lysosomal storage disease | WB:WBGene00020509 | Caenorhabditis elegans | 180533 | hex-1 |
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| DOID:3323 | Sandhoff disease | WB:WBGene00020509 | Caenorhabditis elegans | 180533 | hex-1 |
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| DOID:3320 | Tay-Sachs disease | WB:WBGene00020509 | Caenorhabditis elegans | 180533 | hex-1 |
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| DOID:12377 | spinal muscular atrophy | WB:WBGene00020509 | Caenorhabditis elegans | 180533 | hex-1 |
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| DOID:684 | hepatocellular carcinoma | WB:WBGene00020557 | Caenorhabditis elegans | 172232 | aprt-1 |
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| DOID:0060350 | adenine phosphoribosyltransferase deficiency | WB:WBGene00020557 | Caenorhabditis elegans | 172232 | aprt-1 |
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| DOID:0081326 | oxoglutarate dehydrogenase deficiency | WB:WBGene00020679 | Caenorhabditis elegans | 177235 | ogdh-1 |
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| DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | WB:WBGene00020679 | Caenorhabditis elegans | 177235 | ogdh-1 |
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| DOID:0080563 | congenital disorder of glycosylation Ik | WB:WBGene00020820 | Caenorhabditis elegans | 175920 | algn-1 |
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| DOID:5212 | congenital disorder of glycosylation | WB:WBGene00020820 | Caenorhabditis elegans | 175920 | algn-1 |
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| DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00020820 | Caenorhabditis elegans | 175920 | algn-1 |
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| DOID:0110284 | autosomal recessive limb-girdle muscular dystrophy type 2L | WB:WBGene00020924 | Caenorhabditis elegans | 189104 | W02B3.4 |
|
||
| DOID:0112379 | muscular dystrophy-dystroglycanopathy type B4 | WB:WBGene00020924 | Caenorhabditis elegans | 189104 | W02B3.4 |
|
||
| DOID:9884 | muscular dystrophy | WB:WBGene00020924 | Caenorhabditis elegans | 189104 | W02B3.4 |
|
||
| DOID:0110444 | dilated cardiomyopathy 1X | WB:WBGene00020924 | Caenorhabditis elegans | 189104 | W02B3.4 |
|
||
| DOID:0050560 | Walker-Warburg syndrome | WB:WBGene00020924 | Caenorhabditis elegans | 189104 | W02B3.4 |
|
