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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:0070253 | congenital disorder of glycosylation type IIa | Xenbase:XB-GENE-17345473 | Xenopus laevis (African clawed frog) | 444674 | mgat2.S |
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| DOID:0070253 | congenital disorder of glycosylation type IIa | Xenbase:XB-GENE-978789 | Xenopus tropicalis (tropical clawed frog) | 448439 | mgat2 |
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| DOID:0070253 | congenital disorder of glycosylation type IIa | FB:FBgn0039738 | Drosophila melanogaster (fruit fly) | 43563 | Mgat2 | CG7921 |
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| DOID:0070253 | congenital disorder of glycosylation type IIa | WB:WBGene00001645 | Caenorhabditis elegans | 179562 | gly-20 |
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| DOID:0070253 | congenital disorder of glycosylation type IIa | MGI:2384966 | Mus musculus (house mouse) | 217664 | Mgat2 |
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| DOID:0070253 | congenital disorder of glycosylation type IIa | Xenbase:XB-GENE-978795 | Xenopus laevis (African clawed frog) | 414590 | mgat2.L |
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| DOID:0070253 | congenital disorder of glycosylation type IIa | HGNC:7045 | Homo sapiens (human) | 4247 | MGAT2 |
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| DOID:0070238 | primary coenzyme Q10 deficiency 1 | MGI:1919133 | Mus musculus (house mouse) | 71883 | Coq2 |
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| DOID:0070238 | primary coenzyme Q10 deficiency 1 | RGD:1306722 | Rattus norvegicus (Norway rat) | 498332 | Coq2 |
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| DOID:0070238 | primary coenzyme Q10 deficiency 1 | HGNC:25223 | Homo sapiens (human) | 27235 | COQ2 |
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| DOID:0070221 | progressive familial intrahepatic cholestasis | HGNC:10741 | Homo sapiens (human) | 8482 | SEMA7A |
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| DOID:0070218 | familial hyperinsulinemic hypoglycemia 2 | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:0070218 | familial hyperinsulinemic hypoglycemia 2 | MGI:107501 | Mus musculus (house mouse) | 16514 | Kcnj11 |
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| DOID:0070218 | familial hyperinsulinemic hypoglycemia 2 | RGD:69247 | Rattus norvegicus (Norway rat) | 83535 | Kcnj11 |
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| DOID:0070216 | familial hyperinsulinemic hypoglycemia 3 | RGD:2670 | Rattus norvegicus (Norway rat) | 24385 | Gck |
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| DOID:0070216 | familial hyperinsulinemic hypoglycemia 3 | SGD:S000002924 | Saccharomyces cerevisiae S288C | 852128 | EMI2 |
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| DOID:0070216 | familial hyperinsulinemic hypoglycemia 3 | FB:FBgn0042711 | Drosophila melanogaster (fruit fly) | 117364 | Hex-t1 |
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| DOID:0070216 | familial hyperinsulinemic hypoglycemia 3 | SGD:S000000545 | Saccharomyces cerevisiae S288C | 850317 | GLK1 |
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| DOID:0070216 | familial hyperinsulinemic hypoglycemia 3 | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:0070216 | familial hyperinsulinemic hypoglycemia 3 | MGI:1270854 | Mus musculus (house mouse) | 103988 | Gck |
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| DOID:0070216 | familial hyperinsulinemic hypoglycemia 3 | SGD:S000003222 | Saccharomyces cerevisiae S288C | 852639 | HXK2 |
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| DOID:0070216 | familial hyperinsulinemic hypoglycemia 3 | SGD:S000001949 | Saccharomyces cerevisiae S288C | 850614 | HXK1 |
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| DOID:0070216 | familial hyperinsulinemic hypoglycemia 3 | FB:FBgn0042710 | Drosophila melanogaster (fruit fly) | 43191 | Hex-t2 |
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| DOID:0070215 | familial hyperinsulinemic hypoglycemia 4 | HGNC:4799 | Homo sapiens (human) | 3033 | HADH |
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| DOID:0070199 | Miyoshi muscular dystrophy 1 | MGI:1349385 | Mus musculus (house mouse) | 26903 | Dysf |
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