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:3883 | Lynch syndrome | SGD:S000000695 | Saccharomyces cerevisiae S288C | 850462 | GIT1 |
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DOID:2841 | asthma | SGD:S000000695 | Saccharomyces cerevisiae S288C | 850462 | GIT1 |
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DOID:6000 | congestive heart failure | SGD:S000000695 | Saccharomyces cerevisiae S288C | 850462 | GIT1 |
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DOID:9351 | diabetes mellitus | SGD:S000000695 | Saccharomyces cerevisiae S288C | 850462 | GIT1 |
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DOID:0112182 | mismatch repair cancer syndrome | SGD:S000000695 | Saccharomyces cerevisiae S288C | 850462 | GIT1 |
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DOID:8778 | Crohn's disease | SGD:S000000695 | Saccharomyces cerevisiae S288C | 850462 | GIT1 |
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DOID:14365 | systemic primary carnitine deficiency disease | SGD:S000000695 | Saccharomyces cerevisiae S288C | 850462 | GIT1 |
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DOID:1920 | hyperuricemia | SGD:S000000695 | Saccharomyces cerevisiae S288C | 850462 | GIT1 |
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DOID:783 | end stage renal disease | SGD:S000000695 | Saccharomyces cerevisiae S288C | 850462 | GIT1 |
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DOID:0050908 | myelodysplastic syndrome | SGD:S000000695 | Saccharomyces cerevisiae S288C | 850462 | GIT1 |
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DOID:3021 | acute kidney failure | SGD:S000000695 | Saccharomyces cerevisiae S288C | 850462 | GIT1 |
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DOID:13619 | extrahepatic cholestasis | SGD:S000000695 | Saccharomyces cerevisiae S288C | 850462 | GIT1 |
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DOID:1074 | kidney failure | SGD:S000000695 | Saccharomyces cerevisiae S288C | 850462 | GIT1 |
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DOID:0050570 | congenital disorder of glycosylation type I | SGD:S000001849 | Saccharomyces cerevisiae S288C | 850499 | SEC53 |
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DOID:5212 | congenital disorder of glycosylation | SGD:S000001849 | Saccharomyces cerevisiae S288C | 850499 | SEC53 |
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DOID:0080552 | congenital disorder of glycosylation Ia | SGD:S000001849 | Saccharomyces cerevisiae S288C | 850499 | SEC53 |
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DOID:5154 | borna disease | HGNC:8605 | Homo sapiens (human) | 8505 | PARG |
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DOID:0070352 | stress-induced childhood-onset neurodegeneration with variable ataxia and seizures | HGNC:8605 | Homo sapiens (human) | 8505 | PARG |
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DOID:3454 | brain infarction | HGNC:8605 | Homo sapiens (human) | 8505 | PARG |
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DOID:0111403 | mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations | SGD:S000001861 | Saccharomyces cerevisiae S288C | 850511 | RIM15 |
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DOID:1588 | thrombocytopenia | SGD:S000001861 | Saccharomyces cerevisiae S288C | 850511 | RIM15 |
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DOID:0070394 | developmental and epileptic encephalopathy 108 | SGD:S000001861 | Saccharomyces cerevisiae S288C | 850511 | RIM15 |
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DOID:0050671 | female breast cancer | SGD:S000001861 | Saccharomyces cerevisiae S288C | 850511 | RIM15 |
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DOID:4621 | holoprosencephaly | SGD:S000001869 | Saccharomyces cerevisiae S288C | 850519 | BST1 |
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DOID:3534 | Lafora disease | SGD:S000001911 | Saccharomyces cerevisiae S288C | 850569 | GSY1 |
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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