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:0060256 | Dowling-Degos disease | WB:WBGene00015793 | Caenorhabditis elegans | 180607 | pfut-1 |
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DOID:2747 | glycogen storage disease | WB:WBGene00015754 | Caenorhabditis elegans | 176149 | C14B9.8 |
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DOID:0111042 | glycogen storage disease IXa | WB:WBGene00015754 | Caenorhabditis elegans | 176149 | C14B9.8 |
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DOID:0050545 | visceral heterotaxy | WB:WBGene00015754 | Caenorhabditis elegans | 176149 | C14B9.8 |
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DOID:1459 | hypothyroidism | WB:WBGene00015754 | Caenorhabditis elegans | 176149 | C14B9.8 |
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DOID:0111040 | glycogen storage disease IXd | WB:WBGene00015754 | Caenorhabditis elegans | 176149 | C14B9.8 |
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DOID:0070311 | oligoasthenoteratozoospermia | WB:WBGene00015204 | Caenorhabditis elegans | 174243 | B0495.5 |
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DOID:0080567 | congenital disorder of glycosylation Ip | WB:WBGene00015162 | Caenorhabditis elegans | 176032 | algn-11 |
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DOID:0111459 | classic galactosemia | WB:WBGene00014203 | Caenorhabditis elegans | 175506 | ZK1058.3 |
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DOID:9870 | galactosemia | WB:WBGene00014203 | Caenorhabditis elegans | 175506 | ZK1058.3 |
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DOID:0110170 | Charcot-Marie-Tooth disease axonal type 2Q | WB:WBGene00014098 | Caenorhabditis elegans | 179674 | ogdh-2 |
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DOID:0111453 | 2-aminoadipic 2-oxoadipic aciduria | WB:WBGene00014098 | Caenorhabditis elegans | 179674 | ogdh-2 |
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DOID:0080554 | congenital disorder of glycosylation Ib | WB:WBGene00014013 | Caenorhabditis elegans | 176388 | ZK632.4 |
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DOID:2978 | carbohydrate metabolic disorder | WB:WBGene00014013 | Caenorhabditis elegans | 176388 | ZK632.4 |
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DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00014013 | Caenorhabditis elegans | 176388 | ZK632.4 |
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DOID:0080562 | congenital disorder of glycosylation Ij | WB:WBGene00013362 | Caenorhabditis elegans | 190436 | algn-7 |
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DOID:0110676 | congenital myasthenic syndrome 13 | WB:WBGene00013362 | Caenorhabditis elegans | 190436 | algn-7 |
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DOID:0060759 | immunodeficiency with hyper IgM type 5 | WB:WBGene00013241 | Caenorhabditis elegans | 176633 | ung-1 |
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DOID:11702 | dysgammaglobulinemia | WB:WBGene00013241 | Caenorhabditis elegans | 176633 | ung-1 |
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DOID:14500 | fucosidosis | WB:WBGene00012225 | Caenorhabditis elegans | 189173 | W03G11.3 |
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DOID:9352 | type 2 diabetes mellitus | WB:WBGene00012225 | Caenorhabditis elegans | 189173 | W03G11.3 |
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DOID:9744 | type 1 diabetes mellitus | WB:WBGene00012225 | Caenorhabditis elegans | 189173 | W03G11.3 |
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DOID:8947 | diabetic retinopathy | WB:WBGene00012225 | Caenorhabditis elegans | 189173 | W03G11.3 |
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DOID:9351 | diabetes mellitus | WB:WBGene00012225 | Caenorhabditis elegans | 189173 | W03G11.3 |
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DOID:9352 | type 2 diabetes mellitus | WB:WBGene00012031 | Caenorhabditis elegans | 172509 | gpdh-3 |
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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