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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:1682 | congenital heart disease | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:1682 | congenital heart disease | RGD:1305159 | Rattus norvegicus (Norway rat) | 362093 | Wdr5 |
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| DOID:589 | congenital hemolytic anemia | RGD:2727 | Rattus norvegicus (Norway rat) | 292804 | Gpi |
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| DOID:589 | congenital hemolytic anemia | FB:FBgn0003074 | Drosophila melanogaster (fruit fly) | 35886 | Pgi |
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| DOID:589 | congenital hemolytic anemia | SGD:S000000400 | Saccharomyces cerevisiae S288C | 852495 | PGI1 |
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| DOID:589 | congenital hemolytic anemia | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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| DOID:589 | congenital hemolytic anemia | MGI:95797 | Mus musculus (house mouse) | 14751 | Gpi1 |
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| DOID:0050328 | congenital hypothyroidism | FB:FBgn0004057 | Drosophila melanogaster (fruit fly) | 32974 | Zw |
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| DOID:0050328 | congenital hypothyroidism | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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| DOID:0050328 | congenital hypothyroidism | MGI:105977 | Mus musculus (house mouse) | 14380 | G6pd2 |
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| DOID:0050328 | congenital hypothyroidism | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:0050328 | congenital hypothyroidism | MGI:105979 | Mus musculus (house mouse) | 14381 | G6pdx |
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| DOID:0050328 | congenital hypothyroidism | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:0050328 | congenital hypothyroidism | MGI:1342774 | Mus musculus (house mouse) | 19017 | Ppargc1a |
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| DOID:0050328 | congenital hypothyroidism | RGD:620925 | Rattus norvegicus (Norway rat) | 83516 | Ppargc1a |
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| DOID:0050328 | congenital hypothyroidism | SGD:S000005185 | Saccharomyces cerevisiae S288C | 855480 | ZWF1 |
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| DOID:0050328 | congenital hypothyroidism | RGD:2645 | Rattus norvegicus (Norway rat) | 24377 | G6pd |
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| DOID:0111646 | congenital lactase deficiency | HGNC:6530 | Homo sapiens (human) | 3938 | LCT |
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| DOID:0111334 | congenital leptin deficiency | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:0111334 | congenital leptin deficiency | RGD:3000 | Rattus norvegicus (Norway rat) | 25608 | Lep |
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| DOID:0111334 | congenital leptin deficiency | MGI:104663 | Mus musculus (house mouse) | 16846 | Lep |
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| DOID:0050557 | congenital muscular dystrophy | HGNC:2211 | Homo sapiens (human) | 1291 | COL6A1 |
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| DOID:0050557 | congenital muscular dystrophy | MGI:88459 | Mus musculus (house mouse) | 12833 | Col6a1 |
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| DOID:0080197 | congenital muscular dystrophy with cataracts and intellectual disability | HGNC:33882 | Homo sapiens (human) | 51763 | INPP5K |
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| DOID:0111233 | congenital muscular dystrophy-dystroglycanopathy A14 | HGNC:22932 | Homo sapiens (human) | 29925 | GMPPB |
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