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:11054 | urinary bladder cancer | MGI:97250 | Mus musculus (house mouse) | 17869 | Myc |
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DOID:9970 | obesity | MGI:97250 | Mus musculus (house mouse) | 17869 | Myc |
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DOID:3969 | thyroid gland papillary carcinoma | MGI:97250 | Mus musculus (house mouse) | 17869 | Myc |
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DOID:2526 | prostate adenocarcinoma | MGI:97250 | Mus musculus (house mouse) | 17869 | Myc |
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DOID:127 | leiomyoma | MGI:97250 | Mus musculus (house mouse) | 17869 | Myc |
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DOID:0060318 | acute promyelocytic leukemia | MGI:97250 | Mus musculus (house mouse) | 17869 | Myc |
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DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00019276 | Caenorhabditis elegans | 178822 | algn-5 |
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DOID:0080322 | polycystic kidney disease | WB:WBGene00019276 | Caenorhabditis elegans | 178822 | algn-5 |
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DOID:0080201 | Peters plus syndrome | WB:WBGene00022576 | Caenorhabditis elegans | 178968 | ZC250.2 |
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DOID:9675 | pulmonary emphysema | WB:WBGene00001508 | Caenorhabditis elegans | 178985 | fut-8 |
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DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00022629 | Caenorhabditis elegans | 179185 | algn-12 |
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DOID:0080559 | congenital disorder of glycosylation Ig | WB:WBGene00022629 | Caenorhabditis elegans | 179185 | algn-12 |
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DOID:0080558 | congenital disorder of glycosylation If | WB:WBGene00018181 | Caenorhabditis elegans | 179218 | mpdu-1 |
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DOID:0014667 | disease of metabolism | WB:WBGene00008230 | Caenorhabditis elegans | 179335 | pfk-1.2 |
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DOID:2747 | glycogen storage disease | 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:0112319 | Kanzaki disease | MGI:1261422 | Mus musculus (house mouse) | 17939 | Naga |
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DOID:2367 | neuroaxonal dystrophy | MGI:1261422 | Mus musculus (house mouse) | 17939 | Naga |
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DOID:479 | angiokeratoma | MGI:1261422 | Mus musculus (house mouse) | 17939 | Naga |
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DOID:0112318 | Schindler disease type 1 | MGI:1261422 | Mus musculus (house mouse) | 17939 | Naga |
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DOID:14499 | Fabry disease | MGI:1261422 | Mus musculus (house mouse) | 17939 | Naga |
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DOID:0070253 | congenital disorder of glycosylation type IIa | WB:WBGene00001645 | Caenorhabditis elegans | 179562 | gly-20 |
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DOID:2978 | carbohydrate metabolic disorder | WB:WBGene00001645 | Caenorhabditis elegans | 179562 | gly-20 |
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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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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