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:10652 | Alzheimer's disease | ZFIN:ZDB-GENE-030131-3955 | Danio rerio (zebrafish) | 560788 | parp1 |
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DOID:848 | arthritis | ZFIN:ZDB-GENE-030131-3955 | Danio rerio (zebrafish) | 560788 | parp1 |
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DOID:9352 | type 2 diabetes mellitus | ZFIN:ZDB-GENE-030131-3955 | Danio rerio (zebrafish) | 560788 | parp1 |
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DOID:2747 | glycogen storage disease | WB:WBGene00022199 | Caenorhabditis elegans | 180583 | pfk-1.1 |
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DOID:11721 | glycogen storage disease VII | WB:WBGene00022199 | Caenorhabditis elegans | 180583 | pfk-1.1 |
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DOID:0014667 | disease of metabolism | WB:WBGene00022199 | Caenorhabditis elegans | 180583 | pfk-1.1 |
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DOID:0014667 | disease of metabolism | WB:WBGene00008230 | Caenorhabditis elegans | 179335 | pfk-1.2 |
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DOID:2747 | glycogen storage disease | WB:WBGene00008230 | Caenorhabditis elegans | 179335 | pfk-1.2 |
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DOID:11721 | glycogen storage disease VII | WB:WBGene00008230 | Caenorhabditis elegans | 179335 | pfk-1.2 |
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DOID:2018 | hyperinsulinism | WB:WBGene00019295 | Caenorhabditis elegans | 177363 | pfkb-1.2 |
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DOID:0060256 | Dowling-Degos disease | WB:WBGene00015793 | Caenorhabditis elegans | 180607 | pfut-1 |
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DOID:162 | cancer | WB:WBGene00020185 | Caenorhabditis elegans | 171965 | pgk-1 |
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DOID:14330 | Parkinson's disease | WB:WBGene00020185 | Caenorhabditis elegans | 171965 | pgk-1 |
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DOID:583 | hemolytic anemia | WB:WBGene00020185 | Caenorhabditis elegans | 171965 | pgk-1 |
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DOID:0111933 | phosphoglycerate kinase 1 deficiency | WB:WBGene00020185 | Caenorhabditis elegans | 171965 | pgk-1 |
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DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | ZFIN:ZDB-GENE-040426-1086 | Danio rerio (zebrafish) | 791759 | piga |
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DOID:0060284 | paroxysmal nocturnal hemoglobinuria | Xenbase:XB-GENE-996765 | Xenopus tropicalis (tropical clawed frog) | 100158632 | piga |
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DOID:0060713 | autosomal recessive congenital ichthyosis 4B | ZFIN:ZDB-GENE-040426-1086 | Danio rerio (zebrafish) | 791759 | piga |
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DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | Xenbase:XB-GENE-996765 | Xenopus tropicalis (tropical clawed frog) | 100158632 | piga |
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DOID:0060713 | autosomal recessive congenital ichthyosis 4B | Xenbase:XB-GENE-996765 | Xenopus tropicalis (tropical clawed frog) | 100158632 | piga |
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DOID:0060284 | paroxysmal nocturnal hemoglobinuria | ZFIN:ZDB-GENE-040426-1086 | Danio rerio (zebrafish) | 791759 | piga |
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DOID:0060284 | paroxysmal nocturnal hemoglobinuria | WB:WBGene00008431 | Caenorhabditis elegans | 174386 | piga-1 |
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DOID:0060713 | autosomal recessive congenital ichthyosis 4B | WB:WBGene00008431 | Caenorhabditis elegans | 174386 | piga-1 |
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DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | WB:WBGene00008431 | Caenorhabditis elegans | 174386 | piga-1 |
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DOID:0060284 | paroxysmal nocturnal hemoglobinuria | Xenbase:XB-GENE-6485976 | Xenopus laevis (African clawed frog) | 108707921 | piga.L |
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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