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:0080037 | Worth syndrome | MGI:1278315 | Mus musculus (house mouse) | 16973 | Lrp5 |
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DOID:0080037 | Worth syndrome | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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DOID:14497 | Wolman disease | MGI:96789 | Mus musculus (house mouse) | 16889 | Lipa |
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DOID:14497 | Wolman disease | HGNC:6617 | Homo sapiens (human) | 3988 | LIPA |
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DOID:384 | Wolff-Parkinson-White syndrome | HGNC:9386 | Homo sapiens (human) | 51422 | PRKAG2 |
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DOID:384 | Wolff-Parkinson-White syndrome | MGI:1891343 | Mus musculus (house mouse) | 241113 | Prkag3 |
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DOID:384 | Wolff-Parkinson-White syndrome | MGI:1336153 | Mus musculus (house mouse) | 108099 | Prkag2 |
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DOID:384 | Wolff-Parkinson-White syndrome | HGNC:9387 | Homo sapiens (human) | 53632 | PRKAG3 |
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DOID:893 | Wilson disease | WB:WBGene00000213 | Caenorhabditis elegans | 176879 | asm-3 |
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DOID:893 | Wilson disease | MGI:98325 | Mus musculus (house mouse) | 20597 | Smpd1 |
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DOID:893 | Wilson disease | WB:WBGene00000212 | Caenorhabditis elegans | 181323 | asm-2 |
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DOID:893 | Wilson disease | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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DOID:893 | Wilson disease | WB:WBGene00000211 | Caenorhabditis elegans | 174131 | asm-1 |
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DOID:893 | Wilson disease | HGNC:2606 | Homo sapiens (human) | 1594 | CYP27B1 |
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DOID:893 | Wilson disease | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
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DOID:0050562 | West syndrome | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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DOID:2384 | Wernicke encephalopathy | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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DOID:0050475 | Weill-Marchesani syndrome | MGI:104798 | Mus musculus (house mouse) | 21926 | Tnf |
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DOID:0050475 | Weill-Marchesani syndrome | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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DOID:0050475 | Weill-Marchesani syndrome | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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DOID:0050560 | Walker-Warburg syndrome | Xenbase:XB-GENE-1007367 | Xenopus tropicalis (tropical clawed frog) | 100170600 | b4gat1 |
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DOID:0050560 | Walker-Warburg syndrome | Xenbase:XB-GENE-944435 | Xenopus tropicalis (tropical clawed frog) | 448433 | pomt1 |
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DOID:0050560 | Walker-Warburg syndrome | Xenbase:XB-GENE-1006906 | Xenopus tropicalis (tropical clawed frog) | 100490100 | pomt2 |
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DOID:0050560 | Walker-Warburg syndrome | RGD:1305852 | Rattus norvegicus (Norway rat) | 308390 | Fkrp |
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DOID:0050560 | Walker-Warburg syndrome | HGNC:15685 | Homo sapiens (human) | 11041 | B4GAT1 |
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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