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:3319 | lymphangioleiomyomatosis | SGD:S000003424 | Saccharomyces cerevisiae S288C | 853106 | TDH3 |
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DOID:10652 | Alzheimer's disease | SGD:S000003424 | Saccharomyces cerevisiae S288C | 853106 | TDH3 |
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DOID:3525 | middle cerebral artery infarction | SGD:S000003424 | Saccharomyces cerevisiae S288C | 853106 | TDH3 |
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DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | SGD:S000003431 | Saccharomyces cerevisiae S288C | 853113 | PMT6 |
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DOID:0110298 | autosomal recessive limb-girdle muscular dystrophy type 2N | SGD:S000003431 | Saccharomyces cerevisiae S288C | 853113 | PMT6 |
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DOID:0050453 | lissencephaly | SGD:S000003431 | Saccharomyces cerevisiae S288C | 853113 | PMT6 |
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DOID:9884 | muscular dystrophy | SGD:S000003431 | Saccharomyces cerevisiae S288C | 853113 | PMT6 |
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DOID:0050560 | Walker-Warburg syndrome | SGD:S000003431 | Saccharomyces cerevisiae S288C | 853113 | PMT6 |
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DOID:0111240 | congenital muscular dystrophy-dystroglycanopathy type A2 | SGD:S000003431 | Saccharomyces cerevisiae S288C | 853113 | PMT6 |
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DOID:0112380 | muscular dystrophy-dystroglycanopathy type B2 | SGD:S000003431 | Saccharomyces cerevisiae S288C | 853113 | PMT6 |
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DOID:0112374 | muscular dystrophy-dystroglycanopathy | SGD:S000003431 | Saccharomyces cerevisiae S288C | 853113 | PMT6 |
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DOID:0112213 | multiple congenital anomalies-hypotonia-seizures syndrome 4 | SGD:S000003448 | Saccharomyces cerevisiae S288C | 853130 | GPI1 |
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DOID:0110739 | neurodegeneration with brain iron accumulation 5 | SGD:S000003455 | Saccharomyces cerevisiae S288C | 853138 | HSV2 |
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DOID:0110645 | long QT syndrome 2 | SGD:S000003459 | Saccharomyces cerevisiae S288C | 853142 | DIE2 |
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DOID:0050563 | nonsyndromic deafness | SGD:S000003459 | Saccharomyces cerevisiae S288C | 853142 | DIE2 |
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DOID:2747 | glycogen storage disease | SGD:S000003472 | Saccharomyces cerevisiae S288C | 853155 | PFK1 |
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DOID:11721 | glycogen storage disease VII | SGD:S000003472 | Saccharomyces cerevisiae S288C | 853155 | PFK1 |
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DOID:0014667 | disease of metabolism | SGD:S000003472 | Saccharomyces cerevisiae S288C | 853155 | PFK1 |
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DOID:10652 | Alzheimer's disease | SGD:S000003486 | Saccharomyces cerevisiae S288C | 853169 | ENO1 |
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DOID:11054 | urinary bladder cancer | SGD:S000003486 | Saccharomyces cerevisiae S288C | 853169 | ENO1 |
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DOID:1800 | neuroendocrine carcinoma | SGD:S000003486 | Saccharomyces cerevisiae S288C | 853169 | ENO1 |
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DOID:936 | brain disease | SGD:S000003486 | Saccharomyces cerevisiae S288C | 853169 | ENO1 |
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DOID:3459 | breast carcinoma | SGD:S000003486 | Saccharomyces cerevisiae S288C | 853169 | ENO1 |
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DOID:0080855 | Parkinsonism | SGD:S000003486 | Saccharomyces cerevisiae S288C | 853169 | ENO1 |
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DOID:1712 | aortic valve stenosis | SGD:S000003486 | Saccharomyces cerevisiae S288C | 853169 | ENO1 |
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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