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:0080998 | acute necrotizing pancreatitis | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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DOID:2349 | arteriosclerosis | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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DOID:9477 | pulmonary embolism | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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DOID:2921 | glomerulonephritis | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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DOID:2978 | carbohydrate metabolic disorder | HGNC:11559 | Homo sapiens (human) | 6888 | TALDO1 |
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DOID:2978 | carbohydrate metabolic disorder | SGD:S000004346 | Saccharomyces cerevisiae S288C | 851068 | TAL1 |
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DOID:0050559 | Fukuyama congenital muscular dystrophy | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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DOID:0110443 | dilated cardiomyopathy 1B | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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DOID:0110296 | autosomal recessive limb-girdle muscular dystrophy type 2M | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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DOID:9884 | muscular dystrophy | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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DOID:0110284 | autosomal recessive limb-girdle muscular dystrophy type 2L | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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DOID:0110444 | dilated cardiomyopathy 1X | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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DOID:0112379 | muscular dystrophy-dystroglycanopathy type B4 | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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DOID:0050560 | Walker-Warburg syndrome | WB:WBGene00020307 | Caenorhabditis elegans | 173469 | T07D3.4 |
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DOID:0110296 | autosomal recessive limb-girdle muscular dystrophy type 2M | WB:WBGene00011554 | Caenorhabditis elegans | 188207 | T07A5.1 |
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DOID:0110284 | autosomal recessive limb-girdle muscular dystrophy type 2L | WB:WBGene00011554 | Caenorhabditis elegans | 188207 | T07A5.1 |
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DOID:9884 | muscular dystrophy | WB:WBGene00011554 | Caenorhabditis elegans | 188207 | T07A5.1 |
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DOID:0112379 | muscular dystrophy-dystroglycanopathy type B4 | WB:WBGene00011554 | Caenorhabditis elegans | 188207 | T07A5.1 |
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DOID:0110444 | dilated cardiomyopathy 1X | WB:WBGene00011554 | Caenorhabditis elegans | 188207 | T07A5.1 |
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DOID:0110443 | dilated cardiomyopathy 1B | WB:WBGene00011554 | Caenorhabditis elegans | 188207 | T07A5.1 |
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DOID:0050560 | Walker-Warburg syndrome | WB:WBGene00011554 | Caenorhabditis elegans | 188207 | T07A5.1 |
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DOID:0050559 | Fukuyama congenital muscular dystrophy | WB:WBGene00011554 | Caenorhabditis elegans | 188207 | T07A5.1 |
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DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | WB:WBGene00011554 | Caenorhabditis elegans | 188207 | T07A5.1 |
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DOID:0080572 | congenital disorder of glycosylation Iw | MGI:1915542 | Mus musculus (house mouse) | 68292 | Stt3b |
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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