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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:0090005 | Schwartz-Jampel syndrome 1 | FB:FBgn0284408 | Drosophila melanogaster (fruit fly) | 45320 | trol | CG33950 |
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| DOID:0090005 | Schwartz-Jampel syndrome 1 | HGNC:5273 | Homo sapiens (human) | 3339 | HSPG2 |
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| DOID:0090031 | D-bifunctional protein deficiency | HGNC:5213 | Homo sapiens (human) | 3295 | HSD17B4 |
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| DOID:0090032 | Silverman-Handmaker type dyssegmental dysplasia | FB:FBgn0284408 | Drosophila melanogaster (fruit fly) | 45320 | trol | CG33950 |
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| DOID:0090032 | Silverman-Handmaker type dyssegmental dysplasia | HGNC:5273 | Homo sapiens (human) | 3339 | HSPG2 |
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| DOID:0090044 | dystonia 9 | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:0090045 | childhood onset GLUT1 deficiency syndrome 2 | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:0090056 | dystonia 12 | MGI:88107 | Mus musculus (house mouse) | 232975 | Atp1a3 |
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| DOID:0090056 | dystonia 12 | HGNC:9039 | Homo sapiens (human) | 8398 | PLA2G6 |
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| DOID:0090064 | familial cold autoinflammatory syndrome 3 | HGNC:9066 | Homo sapiens (human) | 5336 | PLCG2 |
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| DOID:0090075 | hypogonadotropic hypogonadism 15 with or without anosmia | FB:FBgn0038755 | Drosophila melanogaster (fruit fly) | 42380 | Hs6st | CG4451 |
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| DOID:0090075 | hypogonadotropic hypogonadism 15 with or without anosmia | ZFIN:ZDB-GENE-070103-2 | Danio rerio (zebrafish) | 791107 | hs6st1b |
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| DOID:0090075 | hypogonadotropic hypogonadism 15 with or without anosmia | ZFIN:ZDB-GENE-050524-1 | Danio rerio (zebrafish) | 553162 | hs6st1a |
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| DOID:0090075 | hypogonadotropic hypogonadism 15 with or without anosmia | Xenbase:XB-GENE-953845 | Xenopus tropicalis (tropical clawed frog) | 550071 | hs6st1 |
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| DOID:0090075 | hypogonadotropic hypogonadism 15 with or without anosmia | RGD:1309218 | Rattus norvegicus (Norway rat) | 316325 | Hs6st1 |
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| DOID:0090075 | hypogonadotropic hypogonadism 15 with or without anosmia | Xenbase:XB-GENE-953851 | Xenopus laevis (African clawed frog) | 373566 | hs6st1.S |
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| DOID:0090075 | hypogonadotropic hypogonadism 15 with or without anosmia | MGI:1354958 | Mus musculus (house mouse) | 50785 | Hs6st1 |
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| DOID:0090075 | hypogonadotropic hypogonadism 15 with or without anosmia | HGNC:5201 | Homo sapiens (human) | 9394 | HS6ST1 |
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| DOID:0090075 | hypogonadotropic hypogonadism 15 with or without anosmia | Xenbase:XB-GENE-17335472 | Xenopus laevis (African clawed frog) | 108717161 | hs6st1.L |
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| DOID:0090101 | lethal congenital glycogen storage disease of heart | MGI:1336153 | Mus musculus (house mouse) | 108099 | Prkag2 |
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| DOID:0090101 | lethal congenital glycogen storage disease of heart | HGNC:9386 | Homo sapiens (human) | 51422 | PRKAG2 |
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| DOID:0090101 | lethal congenital glycogen storage disease of heart | HGNC:9387 | Homo sapiens (human) | 53632 | PRKAG3 |
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| DOID:0090101 | lethal congenital glycogen storage disease of heart | MGI:1891343 | Mus musculus (house mouse) | 241113 | Prkag3 |
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| DOID:0090103 | Huntington's disease-like 1 | HGNC:9449 | Homo sapiens (human) | 5621 | PRNP |
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| DOID:0090122 | aromatase excess syndrome | HGNC:2594 | Homo sapiens (human) | 1588 | CYP19A1 |
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