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 | October 9, 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:1064 | cystinosis | WB:WBGene00008052 | Caenorhabditis elegans | 174308 | ctns-1 |
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DOID:0111458 | galactose epimerase deficiency | WB:WBGene00008132 | Caenorhabditis elegans | 173171 | gale-1 |
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DOID:9870 | galactosemia | WB:WBGene00008132 | Caenorhabditis elegans | 173171 | gale-1 |
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DOID:1588 | thrombocytopenia | WB:WBGene00008132 | Caenorhabditis elegans | 173171 | gale-1 |
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DOID:1485 | cystic fibrosis | WB:WBGene00008148 | Caenorhabditis elegans | 177857 | C47E12.3 |
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DOID:2747 | glycogen storage disease | WB:WBGene00008230 | Caenorhabditis elegans | 179335 | pfk-1.2 |
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DOID:0014667 | disease of metabolism | 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:2962 | Cockayne syndrome | WB:WBGene00008403 | Caenorhabditis elegans | 174474 | csa-1 |
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DOID:0060240 | UV-sensitive syndrome | WB:WBGene00008403 | Caenorhabditis elegans | 174474 | csa-1 |
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DOID:0080907 | Cockayne syndrome A | WB:WBGene00008403 | Caenorhabditis elegans | 174474 | csa-1 |
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DOID:0112315 | brain small vessel disease 3 | WB:WBGene00008426 | Caenorhabditis elegans | 3565069 | D2045.9 |
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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 | 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:783 | end stage renal disease | WB:WBGene00008542 | Caenorhabditis elegans | 184107 | scav-6 |
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DOID:891 | progressive myoclonus epilepsy | WB:WBGene00008542 | Caenorhabditis elegans | 184107 | scav-6 |
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DOID:0111019 | cone-rod dystrophy 12 | WB:WBGene00008571 | Caenorhabditis elegans | 181330 | prmn-1 |
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DOID:0070517 | retinal macular dystrophy 2 | WB:WBGene00008571 | Caenorhabditis elegans | 181330 | prmn-1 |
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DOID:0110376 | retinitis pigmentosa 41 | WB:WBGene00008571 | Caenorhabditis elegans | 181330 | prmn-1 |
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DOID:9351 | diabetes mellitus | WB:WBGene00008571 | Caenorhabditis elegans | 181330 | prmn-1 |
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DOID:1681 | heart septal defect | WB:WBGene00008624 | Caenorhabditis elegans | 178267 | crld-1 |
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DOID:0050651 | atrioventricular septal defect | WB:WBGene00008624 | Caenorhabditis elegans | 178267 | crld-1 |
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DOID:1793 | pancreatic cancer | WB:WBGene00008656 | Caenorhabditis elegans | 184307 | lron-5 |
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DOID:11342 | arcus senilis | WB:WBGene00008656 | Caenorhabditis elegans | 184307 | lron-5 |
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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 v4.1.0
Last updated: December 9, 2024