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: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:0080736 | Ehlers-Danlos syndrome musculocontractural type 1 | RGD:1585023 | Rattus norvegicus (Norway rat) | 691394 | Chst14 |
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DOID:1287 | cardiovascular system disease | RGD:1589798 | Rattus norvegicus (Norway rat) | 690987 | Gys1 |
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DOID:3534 | Lafora disease | RGD:1589798 | Rattus norvegicus (Norway rat) | 690987 | Gys1 |
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DOID:3070 | high grade glioma | HGNC:2172 | Homo sapiens (human) | 6900 | CNTN2 |
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DOID:850 | lung disease | HGNC:2172 | Homo sapiens (human) | 6900 | CNTN2 |
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DOID:0111691 | familial adult myoclonic epilepsy 5 | HGNC:2172 | Homo sapiens (human) | 6900 | CNTN2 |
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DOID:0080201 | Peters plus syndrome | RGD:1588723 | Rattus norvegicus (Norway rat) | 689765 | B3glct |
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DOID:5082 | liver cirrhosis | MGI:1916211 | Mus musculus (house mouse) | 68961 | Phkg2 |
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DOID:2747 | glycogen storage disease | MGI:1916211 | Mus musculus (house mouse) | 68961 | Phkg2 |
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DOID:0111043 | glycogen storage disease IXc | MGI:1916211 | Mus musculus (house mouse) | 68961 | Phkg2 |
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DOID:2978 | carbohydrate metabolic disorder | HGNC:11559 | Homo sapiens (human) | 6888 | TALDO1 |
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DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | RGD:1586427 | Rattus norvegicus (Norway rat) | 688673 | Pomt2 |
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DOID:0050560 | Walker-Warburg syndrome | RGD:1586427 | Rattus norvegicus (Norway rat) | 688673 | Pomt2 |
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DOID:0111240 | congenital muscular dystrophy-dystroglycanopathy type A2 | RGD:1586427 | Rattus norvegicus (Norway rat) | 688673 | Pomt2 |
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DOID:0110298 | autosomal recessive limb-girdle muscular dystrophy type 2N | RGD:1586427 | Rattus norvegicus (Norway rat) | 688673 | Pomt2 |
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DOID:0112374 | muscular dystrophy-dystroglycanopathy | RGD:1586427 | Rattus norvegicus (Norway rat) | 688673 | Pomt2 |
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DOID:0050453 | lissencephaly | RGD:1586427 | Rattus norvegicus (Norway rat) | 688673 | Pomt2 |
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DOID:9884 | muscular dystrophy | RGD:1586427 | Rattus norvegicus (Norway rat) | 688673 | Pomt2 |
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DOID:0112380 | muscular dystrophy-dystroglycanopathy type B2 | RGD:1586427 | Rattus norvegicus (Norway rat) | 688673 | Pomt2 |
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DOID:1793 | pancreatic cancer | RGD:1590210 | Rattus norvegicus (Norway rat) | 685758 | A4gnt |
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DOID:14735 | hereditary angioedema | RGD:1584381 | Rattus norvegicus (Norway rat) | 684979 | Hs3st6 |
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DOID:0111626 | D-glyceric aciduria | RGD:1591498 | Rattus norvegicus (Norway rat) | 684314 | Glyctk |
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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