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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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID ▼ | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0050445 | X-linked dominant hypophosphatemic rickets | HGNC:22140 | Homo sapiens (human) | 56975 | FAM20C |
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| DOID:0050445 | X-linked dominant hypophosphatemic rickets | MGI:2136853 | Mus musculus (house mouse) | 80752 | Fam20c |
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| DOID:0050441 | mucosulfatidosis | MGI:1889844 | Mus musculus (house mouse) | 58911 | Sumf1 |
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| DOID:0050441 | mucosulfatidosis | HGNC:20376 | Homo sapiens (human) | 285362 | SUMF1 |
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| DOID:0050440 | familial partial lipodystrophy | MGI:87934 | Mus musculus (house mouse) | 11551 | Adra2a |
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| DOID:0050440 | familial partial lipodystrophy | RGD:2056 | Rattus norvegicus (Norway rat) | 25083 | Adra2a |
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| DOID:0050440 | familial partial lipodystrophy | MGI:96794 | Mus musculus (house mouse) | 16905 | Lmna |
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| DOID:0050440 | familial partial lipodystrophy | HGNC:9236 | Homo sapiens (human) | 5468 | PPARG |
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| DOID:0050440 | familial partial lipodystrophy | HGNC:281 | Homo sapiens (human) | 150 | ADRA2A |
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| DOID:0050440 | familial partial lipodystrophy | RGD:3371 | Rattus norvegicus (Norway rat) | 25664 | Pparg |
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| DOID:0050440 | familial partial lipodystrophy | MGI:97747 | Mus musculus (house mouse) | 19016 | Pparg |
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| DOID:0050440 | familial partial lipodystrophy | HGNC:6636 | Homo sapiens (human) | 4000 | LMNA |
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| DOID:0050439 | Usher syndrome | MGI:1341292 | Mus musculus (house mouse) | 22283 | Ush2a |
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| DOID:0050439 | Usher syndrome | HGNC:12601 | Homo sapiens (human) | 7399 | USH2A |
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| DOID:0050439 | Usher syndrome | HGNC:24102 | Homo sapiens (human) | 22901 | ARSG |
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| DOID:0050439 | Usher syndrome | RGD:1306571 | Rattus norvegicus (Norway rat) | 303631 | Arsg |
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| DOID:0050439 | Usher syndrome | HGNC:12605 | Homo sapiens (human) | 7401 | CLRN1 |
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| DOID:0050439 | Usher syndrome | HGNC:7606 | Homo sapiens (human) | 4647 | MYO7A |
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| DOID:0050439 | Usher syndrome | MGI:2388124 | Mus musculus (house mouse) | 229320 | Clrn1 |
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| DOID:0050439 | Usher syndrome | MGI:1921258 | Mus musculus (house mouse) | 74008 | Arsg |
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| DOID:0050437 | Danon disease | HGNC:6501 | Homo sapiens (human) | 3920 | LAMP2 |
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| DOID:0050437 | Danon disease | RGD:2990 | Rattus norvegicus (Norway rat) | 24944 | Lamp2 |
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| DOID:0050437 | Danon disease | WB:WBGene00003053 | Caenorhabditis elegans | 180912 | lmp-1 |
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| DOID:0050437 | Danon disease | MGI:96748 | Mus musculus (house mouse) | 16784 | Lamp2 |
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| DOID:0050436 | mulibrey nanism | MGI:2153072 | Mus musculus (house mouse) | 68729 | Trim37 |
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