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 | October 9, 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:0110296 | autosomal recessive limb-girdle muscular dystrophy type 2M | Xenbase:XB-GENE-971788 | Xenopus tropicalis (tropical clawed frog) | 100124956 | fktn |
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DOID:0050560 | Walker-Warburg syndrome | Xenbase:XB-GENE-971788 | Xenopus tropicalis (tropical clawed frog) | 100124956 | fktn |
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DOID:9884 | muscular dystrophy | Xenbase:XB-GENE-971788 | Xenopus tropicalis (tropical clawed frog) | 100124956 | fktn |
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DOID:0110443 | dilated cardiomyopathy 1B | ZFIN:ZDB-GENE-070410-96 | Danio rerio (zebrafish) | 100006345 | fktn |
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DOID:0110444 | dilated cardiomyopathy 1X | Xenbase:XB-GENE-971793 | Xenopus laevis (African clawed frog) | 495324 | fktn.S |
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DOID:0110284 | autosomal recessive limb-girdle muscular dystrophy type 2L | Xenbase:XB-GENE-971793 | Xenopus laevis (African clawed frog) | 495324 | fktn.S |
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DOID:0112379 | muscular dystrophy-dystroglycanopathy type B4 | Xenbase:XB-GENE-971793 | Xenopus laevis (African clawed frog) | 495324 | fktn.S |
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DOID:0110443 | dilated cardiomyopathy 1B | Xenbase:XB-GENE-971793 | Xenopus laevis (African clawed frog) | 495324 | fktn.S |
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DOID:0110296 | autosomal recessive limb-girdle muscular dystrophy type 2M | Xenbase:XB-GENE-971793 | Xenopus laevis (African clawed frog) | 495324 | fktn.S |
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DOID:0050560 | Walker-Warburg syndrome | Xenbase:XB-GENE-971793 | Xenopus laevis (African clawed frog) | 495324 | fktn.S |
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DOID:9884 | muscular dystrophy | Xenbase:XB-GENE-971793 | Xenopus laevis (African clawed frog) | 495324 | fktn.S |
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DOID:0050559 | Fukuyama congenital muscular dystrophy | Xenbase:XB-GENE-971793 | Xenopus laevis (African clawed frog) | 495324 | fktn.S |
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DOID:0090093 | hypogonadotropic hypogonadism 21 with or without anosmia | Xenbase:XB-GENE-490901 | Xenopus tropicalis (tropical clawed frog) | 100144692 | flrt3 |
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DOID:0090093 | hypogonadotropic hypogonadism 21 with or without anosmia | Xenbase:XB-GENE-17334173 | Xenopus laevis (African clawed frog) | 394225 | flrt3.S |
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DOID:0050580 | hereditary lymphedema | WB:WBGene00001475 | Caenorhabditis elegans | 179788 | fmi-1 |
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DOID:10908 | hydrocephalus | WB:WBGene00001475 | Caenorhabditis elegans | 179788 | fmi-1 |
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DOID:0112361 | spondylocostal dysostosis 3 | FB:FBgn0011591 | Drosophila melanogaster (fruit fly) | 40314 | fng | CG10580 |
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DOID:612 | primary immunodeficiency disease | WB:WBGene00007388 | Caenorhabditis elegans | 179544 | folt-1 |
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DOID:12365 | malaria | WB:WBGene00007388 | Caenorhabditis elegans | 179544 | folt-1 |
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DOID:0050659 | biotin-responsive basal ganglia disease | WB:WBGene00007388 | Caenorhabditis elegans | 179544 | folt-1 |
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DOID:7693 | abdominal aortic aneurysm | WB:WBGene00007388 | Caenorhabditis elegans | 179544 | folt-1 |
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DOID:9296 | cleft lip | WB:WBGene00007388 | Caenorhabditis elegans | 179544 | folt-1 |
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DOID:0090117 | thiamine-responsive megaloblastic anemia syndrome | WB:WBGene00007388 | Caenorhabditis elegans | 179544 | folt-1 |
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DOID:784 | chronic kidney disease | WB:WBGene00007388 | Caenorhabditis elegans | 179544 | folt-1 |
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DOID:9351 | diabetes mellitus | WB:WBGene00007388 | Caenorhabditis elegans | 179544 | folt-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 v4.1.0
Last updated: December 9, 2024