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:10763 | hypertension | RGD:620630 | Rattus norvegicus (Norway rat) | 85268 | Hrh3 |
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DOID:1508 | candidiasis | SGD:S000003149 | Saccharomyces cerevisiae S288C | 852694 | GTS1 |
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DOID:0050561 | Lennox-Gastaut syndrome | HGNC:2851 | Homo sapiens (human) | 8527 | DGKD |
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DOID:10652 | Alzheimer's disease | SGD:S000003141 | Saccharomyces cerevisiae S288C | 852702 | XRN1 |
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DOID:10112 | sleeping sickness | SGD:S000003110 | Saccharomyces cerevisiae S288C | 852735 | GPI10 |
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DOID:0112216 | developmental and epileptic encephalopathy 80 | SGD:S000003110 | Saccharomyces cerevisiae S288C | 852735 | GPI10 |
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DOID:9119 | acute myeloid leukemia | SGD:S000003060 | Saccharomyces cerevisiae S288C | 852788 | NUP145 |
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DOID:5603 | T-cell acute lymphoblastic leukemia | SGD:S000003060 | Saccharomyces cerevisiae S288C | 852788 | NUP145 |
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DOID:0060644 | chondrodysplasia-pseudohermaphroditism syndrome | SGD:S000003052 | Saccharomyces cerevisiae S288C | 852796 | GUP1 |
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DOID:0080980 | arthrogryposis multiplex congenita-4 | SGD:S000003051 | Saccharomyces cerevisiae S288C | 852797 | SCY1 |
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DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | SGD:S000003045 | Saccharomyces cerevisiae S288C | 852803 | HNM1 |
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DOID:0111666 | proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome | SGD:S000003045 | Saccharomyces cerevisiae S288C | 852803 | HNM1 |
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DOID:9455 | lipid storage disease | SGD:S000003045 | Saccharomyces cerevisiae S288C | 852803 | HNM1 |
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DOID:12858 | Huntington's disease | SGD:S000003041 | Saccharomyces cerevisiae S288C | 852806 | HSF1 |
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DOID:11383 | cryptorchidism | SGD:S000003041 | Saccharomyces cerevisiae S288C | 852806 | HSF1 |
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DOID:83 | cataract | SGD:S000003041 | Saccharomyces cerevisiae S288C | 852806 | HSF1 |
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DOID:10652 | Alzheimer's disease | SGD:S000003041 | Saccharomyces cerevisiae S288C | 852806 | HSF1 |
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DOID:0110255 | cataract 5 multiple types | SGD:S000003041 | Saccharomyces cerevisiae S288C | 852806 | HSF1 |
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DOID:14330 | Parkinson's disease | SGD:S000003041 | Saccharomyces cerevisiae S288C | 852806 | HSF1 |
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DOID:6000 | congestive heart failure | SGD:S000003041 | Saccharomyces cerevisiae S288C | 852806 | HSF1 |
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DOID:224 | transient cerebral ischemia | SGD:S000003041 | Saccharomyces cerevisiae S288C | 852806 | HSF1 |
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DOID:767 | muscular atrophy | SGD:S000003041 | Saccharomyces cerevisiae S288C | 852806 | HSF1 |
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DOID:0112113 | combined oxidative phosphorylation deficiency 45 | SGD:S000003036 | Saccharomyces cerevisiae S288C | 852811 | MNP1 |
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DOID:0080561 | congenital disorder of glycosylation Ii | SGD:S000003033 | Saccharomyces cerevisiae S288C | 852815 | ALG2 |
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DOID:0110669 | congenital myasthenic syndrome 14 | SGD:S000003033 | Saccharomyces cerevisiae S288C | 852815 | ALG2 |
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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