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:10652 | Alzheimer's disease | HGNC:6470 | Homo sapiens (human) | 3897 | L1CAM |
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DOID:0110292 | autosomal recessive limb-girdle muscular dystrophy type 2O | Xenbase:XB-GENE-959856 | Xenopus tropicalis (tropical clawed frog) | 100158594 | pomgnt1 |
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DOID:3070 | high grade glioma | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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DOID:10223 | dermatomyositis | MGI:1346060 | Mus musculus (house mouse) | 24088 | Tlr2 |
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DOID:3070 | high grade glioma | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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DOID:0110645 | long QT syndrome 2 | WB:WBGene00007043 | Caenorhabditis elegans | 172855 | algn-10 |
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DOID:9970 | obesity | HGNC:10658 | Homo sapiens (human) | 6382 | SDC1 |
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DOID:0060653 | lethal congenital contracture syndrome 3 | HGNC:8996 | Homo sapiens (human) | 23396 | PIP5K1C |
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DOID:6432 | pulmonary hypertension | RGD:708528 | Rattus norvegicus (Norway rat) | 282821 | Has1 |
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DOID:9352 | type 2 diabetes mellitus | FB:FBgn0267385 | Drosophila melanogaster (fruit fly) | 42620 | Pyk |
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DOID:13544 | low tension glaucoma | MGI:104798 | Mus musculus (house mouse) | 21926 | Tnf |
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DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | Xenbase:XB-GENE-6488680 | Xenopus laevis (African clawed frog) | 108699937 | pomt1.S |
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DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | MGI:104663 | Mus musculus (house mouse) | 16846 | Lep |
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DOID:2739 | Gilbert syndrome | ZFIN:ZDB-GENE-040426-2762 | Danio rerio (zebrafish) | 406731 | ugt1ab |
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DOID:10873 | Kuhnt-Junius degeneration | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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DOID:11983 | Prader-Willi syndrome | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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DOID:3908 | lung non-small cell carcinoma | HGNC:2602 | Homo sapiens (human) | 1591 | CYP24A1 |
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DOID:0080556 | congenital disorder of glycosylation Id | SGD:S000000178 | Saccharomyces cerevisiae S288C | 852196 | ALG3 |
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DOID:583 | hemolytic anemia | RGD:619868 | Rattus norvegicus (Norway rat) | 25283 | Gclc |
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DOID:0080488 | mucolipidosis | MGI:97305 | Mus musculus (house mouse) | 18010 | Neu1 |
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DOID:0111402 | mucopolysaccharidosis type IIID | HGNC:4422 | Homo sapiens (human) | 2799 | GNS |
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DOID:9970 | obesity | MGI:1915304 | Mus musculus (house mouse) | 68054 | Serpina12 |
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DOID:9352 | type 2 diabetes mellitus | RGD:2645 | Rattus norvegicus (Norway rat) | 24377 | G6pd |
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DOID:206 | hereditary multiple exostoses | ZFIN:ZDB-GENE-041124-2 | Danio rerio (zebrafish) | 493783 | extl3 |
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DOID:13628 | favism | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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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