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 |
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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 |
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DOID:0060589 | Yunis-Varon syndrome | FB:FBgn0031611 | Drosophila melanogaster (fruit fly) | 33658 | FIG4 |
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DOID:1289 | neurodegenerative disease | SGD:S000005269 | Saccharomyces cerevisiae S288C | 855392 | FIG4 |
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DOID:0080923 | bilateral parasagittal parieto-occipital polymicrogyria | FB:FBgn0031611 | Drosophila melanogaster (fruit fly) | 33658 | FIG4 |
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DOID:0110184 | Charcot-Marie-Tooth disease type 4J | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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DOID:0080923 | bilateral parasagittal parieto-occipital polymicrogyria | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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DOID:0110184 | Charcot-Marie-Tooth disease type 4J | FB:FBgn0031611 | Drosophila melanogaster (fruit fly) | 33658 | FIG4 |
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DOID:0060202 | amyotrophic lateral sclerosis type 11 | SGD:S000005269 | Saccharomyces cerevisiae S288C | 855392 | FIG4 |
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DOID:0060589 | Yunis-Varon syndrome | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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DOID:10595 | Charcot-Marie-Tooth disease | FB:FBgn0031611 | Drosophila melanogaster (fruit fly) | 33658 | FIG4 |
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DOID:0080923 | bilateral parasagittal parieto-occipital polymicrogyria | SGD:S000005269 | Saccharomyces cerevisiae S288C | 855392 | FIG4 |
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DOID:0060202 | amyotrophic lateral sclerosis type 11 | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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DOID:0060589 | Yunis-Varon syndrome | SGD:S000005269 | Saccharomyces cerevisiae S288C | 855392 | FIG4 |
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DOID:1289 | neurodegenerative disease | FB:FBgn0031611 | Drosophila melanogaster (fruit fly) | 33658 | FIG4 |
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DOID:10595 | Charcot-Marie-Tooth disease | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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DOID:10595 | Charcot-Marie-Tooth disease | SGD:S000005269 | Saccharomyces cerevisiae S288C | 855392 | FIG4 |
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DOID:11724 | limb-girdle muscular dystrophy | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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DOID:0110635 | muscular dystrophy-dystroglycanopathy type B5 | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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DOID:12930 | dilated cardiomyopathy | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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DOID:0110299 | autosomal recessive limb-girdle muscular dystrophy type 2I | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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DOID:0111241 | congenital muscular dystrophy-dystroglycanopathy type A5 | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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DOID:0050560 | Walker-Warburg syndrome | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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DOID:9884 | muscular dystrophy | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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DOID:0112379 | muscular dystrophy-dystroglycanopathy type B4 | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024