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:10652 | Alzheimer's disease | Xenbase:XB-GENE-865040 | Xenopus laevis (African clawed frog) | 398022 | igf1r.S |
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DOID:3587 | pancreatic ductal carcinoma | Xenbase:XB-GENE-865040 | Xenopus laevis (African clawed frog) | 398022 | igf1r.S |
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DOID:2871 | endometrial carcinoma | Xenbase:XB-GENE-865047 | Xenopus laevis (African clawed frog) | 397706 | wnt4.L |
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DOID:0111526 | Mullerian aplasia and hyperandrogenism | Xenbase:XB-GENE-865047 | Xenopus laevis (African clawed frog) | 397706 | wnt4.L |
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DOID:0110290 | autosomal recessive limb-girdle muscular dystrophy type 2X | Xenbase:XB-GENE-865066 | Xenopus laevis (African clawed frog) | 779321 | bves.S |
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DOID:5419 | schizophrenia | Xenbase:XB-GENE-865070 | Xenopus laevis (African clawed frog) | 399190 | fzd3.L |
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DOID:1928 | Williams-Beuren syndrome | Xenbase:XB-GENE-865070 | Xenopus laevis (African clawed frog) | 399190 | fzd3.L |
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DOID:0110347 | osteogenesis imperfecta type 15 | Xenbase:XB-GENE-865073 | Xenopus laevis (African clawed frog) | 373578 | wnt1.L |
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DOID:0111650 | ectodermal dysplasia 13 | Xenbase:XB-GENE-865130 | Xenopus laevis (African clawed frog) | 398249 | kremen1.S |
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DOID:0111412 | exudative vitreoretinopathy 1 | Xenbase:XB-GENE-865153 | Xenopus laevis (African clawed frog) | 399192 | fzd4.S |
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DOID:8634 | prostate carcinoma in situ | Xenbase:XB-GENE-865153 | Xenopus laevis (African clawed frog) | 399192 | fzd4.S |
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DOID:14330 | Parkinson's disease | Xenbase:XB-GENE-865228 | Xenopus laevis (African clawed frog) | 398763 | agtr1.L |
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DOID:6713 | cerebrovascular disease | Xenbase:XB-GENE-865228 | Xenopus laevis (African clawed frog) | 398763 | agtr1.L |
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DOID:0060224 | atrial fibrillation | Xenbase:XB-GENE-865228 | Xenopus laevis (African clawed frog) | 398763 | agtr1.L |
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DOID:12858 | Huntington's disease | Xenbase:XB-GENE-865228 | Xenopus laevis (African clawed frog) | 398763 | agtr1.L |
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DOID:12705 | Friedreich ataxia | Xenbase:XB-GENE-865228 | Xenopus laevis (African clawed frog) | 398763 | agtr1.L |
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DOID:784 | chronic kidney disease | Xenbase:XB-GENE-865228 | Xenopus laevis (African clawed frog) | 398763 | agtr1.L |
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DOID:8805 | intermediate coronary syndrome | Xenbase:XB-GENE-865228 | Xenopus laevis (African clawed frog) | 398763 | agtr1.L |
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DOID:5844 | myocardial infarction | Xenbase:XB-GENE-865228 | Xenopus laevis (African clawed frog) | 398763 | agtr1.L |
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DOID:3407 | carotid artery disease | Xenbase:XB-GENE-865228 | Xenopus laevis (African clawed frog) | 398763 | agtr1.L |
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DOID:1612 | breast cancer | Xenbase:XB-GENE-865228 | Xenopus laevis (African clawed frog) | 398763 | agtr1.L |
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DOID:3393 | coronary artery disease | Xenbase:XB-GENE-865228 | Xenopus laevis (African clawed frog) | 398763 | agtr1.L |
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DOID:4450 | renal cell carcinoma | Xenbase:XB-GENE-865228 | Xenopus laevis (African clawed frog) | 398763 | agtr1.L |
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DOID:6432 | pulmonary hypertension | Xenbase:XB-GENE-865228 | Xenopus laevis (African clawed frog) | 398763 | agtr1.L |
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DOID:10825 | essential hypertension | Xenbase:XB-GENE-865228 | Xenopus laevis (African clawed frog) | 398763 | agtr1.L |
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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