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:7693 | abdominal aortic aneurysm | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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DOID:7693 | abdominal aortic aneurysm | HGNC:10720 | Homo sapiens (human) | 6402 | SELL |
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DOID:7693 | abdominal aortic aneurysm | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
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DOID:905 | Zellweger syndrome | HGNC:10606 | Homo sapiens (human) | 6342 | SCP2 |
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DOID:0060589 | Yunis-Varon syndrome | FB:FBgn0031611 | Drosophila melanogaster (fruit fly) | 33658 | FIG4 |
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DOID:0060589 | Yunis-Varon syndrome | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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DOID:0060589 | Yunis-Varon syndrome | SGD:S000005269 | Saccharomyces cerevisiae S288C | 855392 | FIG4 |
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DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | HGNC:8124 | Homo sapiens (human) | 4967 | OGDH |
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DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | Xenbase:XB-GENE-984155 | Xenopus laevis (African clawed frog) | 447370 | ogdhl.L |
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DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | MGI:1098267 | Mus musculus (house mouse) | 18293 | Ogdh |
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DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | HGNC:25590 | Homo sapiens (human) | 55753 | OGDHL |
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DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | RGD:1561359 | Rattus norvegicus (Norway rat) | 360975 | Ogdh |
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DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | WB:WBGene00020679 | Caenorhabditis elegans | 177235 | ogdh-1 |
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DOID:0112105 | X-linked parkinsonism-spasticity syndrome | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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DOID:0112105 | X-linked parkinsonism-spasticity syndrome | FB:FBgn0037671 | Drosophila melanogaster (fruit fly) | 41104 | ATP6AP2 |
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DOID:0080319 | X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia | FB:FBgn0032015 | Drosophila melanogaster (fruit fly) | 34137 | OstĪ³ | CG7830 |
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DOID:0080319 | X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia | FB:FBgn0032015 | Drosophila melanogaster (fruit fly) | 34137 | Ostgamma | CG7830 |
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DOID:0080319 | X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia | SGD:S000005611 | Saccharomyces cerevisiae S288C | 854252 | OST3 |
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DOID:1700 | X-linked ichthyosis | HGNC:11425 | Homo sapiens (human) | 412 | STS |
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DOID:0111739 | X-linked deafness 1 | HGNC:9462 | Homo sapiens (human) | 5631 | PRPS1 |
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DOID:0080352 | X-linked chondrodysplasia punctata 2 | HGNC:3133 | Homo sapiens (human) | 10682 | EBP |
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DOID:0060292 | X-linked chondrodysplasia punctata 1 | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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DOID:0060292 | X-linked chondrodysplasia punctata 1 | HGNC:3133 | Homo sapiens (human) | 10682 | EBP |
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DOID:14179 | X-linked agammaglobulinemia | MGI:97583 | Mus musculus (house mouse) | 18708 | Pik3r1 |
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DOID:14179 | X-linked agammaglobulinemia | RGD:3329 | Rattus norvegicus (Norway rat) | 25513 | Pik3r1 |
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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