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:162 | cancer | SGD:S000001085 | Saccharomyces cerevisiae S288C | 856439 | DOG2 |
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DOID:0080565 | congenital disorder of glycosylation Im | HGNC:23406 | Homo sapiens (human) | 22845 | DOLK |
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DOID:0050570 | congenital disorder of glycosylation type I | HGNC:23406 | Homo sapiens (human) | 22845 | DOLK |
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DOID:0110676 | congenital myasthenic syndrome 13 | HGNC:2995 | Homo sapiens (human) | 1798 | DPAGT1 |
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DOID:0080562 | congenital disorder of glycosylation Ij | HGNC:2995 | Homo sapiens (human) | 1798 | DPAGT1 |
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DOID:687 | hepatoblastoma | HGNC:3002 | Homo sapiens (human) | 1800 | DPEP1 |
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DOID:0050570 | congenital disorder of glycosylation type I | HGNC:3005 | Homo sapiens (human) | 8813 | DPM1 |
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DOID:0080557 | congenital disorder of glycosylation Ie | HGNC:3005 | Homo sapiens (human) | 8813 | DPM1 |
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DOID:0050570 | congenital disorder of glycosylation type I | SGD:S000006387 | Saccharomyces cerevisiae S288C | 856313 | DPM1 |
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DOID:0080557 | congenital disorder of glycosylation Ie | SGD:S000006387 | Saccharomyces cerevisiae S288C | 856313 | DPM1 |
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DOID:1612 | breast cancer | SGD:S000006387 | Saccharomyces cerevisiae S288C | 856313 | DPM1 |
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DOID:0080571 | congenital disorder of glycosylation Iu | HGNC:3006 | Homo sapiens (human) | 8818 | DPM2 |
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DOID:0050570 | congenital disorder of glycosylation type I | HGNC:3007 | Homo sapiens (human) | 54344 | DPM3 |
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DOID:0112376 | muscular dystrophy-dystroglycanopathy type B15 | HGNC:3007 | Homo sapiens (human) | 54344 | DPM3 |
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DOID:0111156 | spermatogenic failure 9 | HGNC:19414 | Homo sapiens (human) | 283417 | DPY19L2 |
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DOID:0080737 | Ehlers-Danlos syndrome musculocontractural type 2 | HGNC:21144 | Homo sapiens (human) | 29940 | DSE |
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DOID:0111258 | pentosuria | MGI:1915130 | Mus musculus (house mouse) | 67880 | Dcxr |
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DOID:0111258 | pentosuria | RGD:620031 | Rattus norvegicus (Norway rat) | 171408 | Dcxr |
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DOID:5844 | myocardial infarction | FB:FBgn0034072 | Drosophila melanogaster (fruit fly) | 36773 | Dg | CG18250 |
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DOID:9884 | muscular dystrophy | FB:FBgn0034072 | Drosophila melanogaster (fruit fly) | 36773 | Dg | CG18250 |
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DOID:12930 | dilated cardiomyopathy | FB:FBgn0034072 | Drosophila melanogaster (fruit fly) | 36773 | Dg | CG18250 |
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DOID:0110293 | autosomal recessive limb-girdle muscular dystrophy type 2P | FB:FBgn0034072 | Drosophila melanogaster (fruit fly) | 36773 | Dg | CG18250 |
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DOID:3429 | inclusion body myositis | FB:FBgn0034072 | Drosophila melanogaster (fruit fly) | 36773 | Dg | CG18250 |
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DOID:767 | muscular atrophy | FB:FBgn0034072 | Drosophila melanogaster (fruit fly) | 36773 | Dg | CG18250 |
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DOID:12236 | primary biliary cholangitis | FB:FBgn0034072 | Drosophila melanogaster (fruit fly) | 36773 | Dg | CG18250 |
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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