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:289 | endometriosis | WB:WBGene00013039 | Caenorhabditis elegans | 176673 | scav-3 |
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DOID:8552 | chronic myeloid leukemia | WB:WBGene00013039 | Caenorhabditis elegans | 176673 | scav-3 |
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DOID:0111444 | progressive myoclonus epilepsy 4 | WB:WBGene00013039 | Caenorhabditis elegans | 176673 | scav-3 |
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DOID:12554 | hemolytic-uremic syndrome | WB:WBGene00013039 | Caenorhabditis elegans | 176673 | scav-3 |
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DOID:10652 | Alzheimer's disease | WB:WBGene00013039 | Caenorhabditis elegans | 176673 | scav-3 |
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DOID:2349 | arteriosclerosis | WB:WBGene00013039 | Caenorhabditis elegans | 176673 | scav-3 |
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DOID:3429 | inclusion body myositis | WB:WBGene00013039 | Caenorhabditis elegans | 176673 | scav-3 |
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DOID:10003 | sensorineural hearing loss | WB:WBGene00013039 | Caenorhabditis elegans | 176673 | scav-3 |
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DOID:0111046 | platelet-type bleeding disorder 10 | WB:WBGene00013039 | Caenorhabditis elegans | 176673 | scav-3 |
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DOID:11702 | dysgammaglobulinemia | WB:WBGene00013241 | Caenorhabditis elegans | 176633 | ung-1 |
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DOID:0060759 | immunodeficiency with hyper IgM type 5 | WB:WBGene00013241 | Caenorhabditis elegans | 176633 | ung-1 |
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DOID:0110676 | congenital myasthenic syndrome 13 | WB:WBGene00013362 | Caenorhabditis elegans | 190436 | algn-7 |
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DOID:0080562 | congenital disorder of glycosylation Ij | WB:WBGene00013362 | Caenorhabditis elegans | 190436 | algn-7 |
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DOID:0111996 | immunodeficiency 51 | WB:WBGene00013415 | Caenorhabditis elegans | 178376 | ilcr-1 |
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DOID:10652 | Alzheimer's disease | WB:WBGene00013446 | Caenorhabditis elegans | 176581 | Y66D12A.21 |
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DOID:0110337 | osteogenesis imperfecta type 7 | WB:WBGene00013531 | Caenorhabditis elegans | 178435 | Y73F8A.26 |
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DOID:0110336 | osteogenesis imperfecta type 8 | WB:WBGene00013531 | Caenorhabditis elegans | 178435 | Y73F8A.26 |
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DOID:12554 | hemolytic-uremic syndrome | WB:WBGene00013578 | Caenorhabditis elegans | 176787 | scav-2 |
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DOID:2224 | essential thrombocythemia | WB:WBGene00013578 | Caenorhabditis elegans | 176787 | scav-2 |
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DOID:10923 | sickle cell anemia | WB:WBGene00013578 | Caenorhabditis elegans | 176787 | scav-2 |
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DOID:8997 | polycythemia vera | WB:WBGene00013578 | Caenorhabditis elegans | 176787 | scav-2 |
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DOID:2957 | pulmonary tuberculosis | WB:WBGene00013578 | Caenorhabditis elegans | 176787 | scav-2 |
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DOID:2218 | blood platelet disease | WB:WBGene00013578 | Caenorhabditis elegans | 176787 | scav-2 |
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DOID:8552 | chronic myeloid leukemia | WB:WBGene00013578 | Caenorhabditis elegans | 176787 | scav-2 |
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DOID:289 | endometriosis | WB:WBGene00013578 | Caenorhabditis elegans | 176787 | scav-2 |
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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