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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:14499 | Fabry disease | HGNC:7631 | Homo sapiens (human) | 4668 | NAGA |
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| DOID:13636 | Fanconi anemia | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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| DOID:13636 | Fanconi anemia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:13636 | Fanconi anemia | MGI:104798 | Mus musculus (house mouse) | 21926 | Tnf |
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| DOID:0080759 | Fanconi renotubular syndrome 3 | HGNC:3247 | Homo sapiens (human) | 1962 | EHHADH |
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| DOID:1062 | Fanconi syndrome | HGNC:11006 | Homo sapiens (human) | 6514 | SLC2A2 |
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| DOID:1062 | Fanconi syndrome | HGNC:2518 | Homo sapiens (human) | 1497 | CTNS |
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| DOID:0050464 | Farber lipogranulomatosis | HGNC:735 | Homo sapiens (human) | 427 | ASAH1 |
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| DOID:0060448 | Fleck corneal dystrophy | HGNC:23785 | Homo sapiens (human) | 200576 | PIKFYVE |
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| DOID:0090001 | Fraser syndrome | HGNC:23399 | Homo sapiens (human) | 158326 | FREM1 |
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| DOID:0050559 | Fukuyama congenital muscular dystrophy | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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| DOID:0050559 | Fukuyama congenital muscular dystrophy | Xenbase:XB-GENE-971788 | Xenopus tropicalis (tropical clawed frog) | 100124956 | fktn |
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| DOID:0050559 | Fukuyama congenital muscular dystrophy | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:0050559 | Fukuyama congenital muscular dystrophy | WB:WBGene00020924 | Caenorhabditis elegans | 189104 | W02B3.4 |
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| DOID:0050559 | Fukuyama congenital muscular dystrophy | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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| DOID:0050559 | Fukuyama congenital muscular dystrophy | MGI:2179507 | Mus musculus (house mouse) | 246179 | Fktn |
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| DOID:0050559 | Fukuyama congenital muscular dystrophy | ZFIN:ZDB-GENE-070410-96 | Danio rerio (zebrafish) | 100006345 | fktn |
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| DOID:0050559 | Fukuyama congenital muscular dystrophy | RGD:1310087 | Rattus norvegicus (Norway rat) | 362520 | Fktn |
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| DOID:0050559 | Fukuyama congenital muscular dystrophy | FB:FBgn0034072 | Drosophila melanogaster (fruit fly) | 36773 | Dg | CG18250 |
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| DOID:0050559 | Fukuyama congenital muscular dystrophy | Xenbase:XB-GENE-971793 | Xenopus laevis (African clawed frog) | 495324 | fktn.S |
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| DOID:0050559 | Fukuyama congenital muscular dystrophy | WB:WBGene00011554 | Caenorhabditis elegans | 188207 | T07A5.1 |
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| DOID:0060174 | GABA aminotransferase deficiency | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:3322 | GM1 gangliosidosis | MGI:88151 | Mus musculus (house mouse) | 12091 | Glb1 |
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| DOID:3322 | GM1 gangliosidosis | HGNC:4298 | Homo sapiens (human) | 2720 | GLB1 |
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| DOID:0080502 | GM1 gangliosidosis type 1 | HGNC:4298 | Homo sapiens (human) | 2720 | GLB1 |
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