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:0080693 | Noonan syndrome-like disorder with loose anagen hair 2 | SGD:S000000935 | Saccharomyces cerevisiae S288C | 856870 | GLC7 |
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DOID:6000 | congestive heart failure | SGD:S000000935 | Saccharomyces cerevisiae S288C | 856870 | GLC7 |
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DOID:162 | cancer | SGD:S000000935 | Saccharomyces cerevisiae S288C | 856870 | GLC7 |
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DOID:9352 | type 2 diabetes mellitus | SGD:S000000935 | Saccharomyces cerevisiae S288C | 856870 | GLC7 |
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DOID:13268 | porphyria | SGD:S000000737 | Saccharomyces cerevisiae S288C | 856705 | GLC3 |
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DOID:2957 | pulmonary tuberculosis | SGD:S000000737 | Saccharomyces cerevisiae S288C | 856705 | GLC3 |
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DOID:2750 | glycogen storage disease IV | SGD:S000000737 | Saccharomyces cerevisiae S288C | 856705 | GLC3 |
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DOID:12804 | mucopolysaccharidosis IV | HGNC:4298 | Homo sapiens (human) | 2720 | GLB1 |
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DOID:0080502 | GM1 gangliosidosis type 1 | HGNC:4298 | Homo sapiens (human) | 2720 | GLB1 |
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DOID:0111392 | mucopolysaccharidosis type IVB | HGNC:4298 | Homo sapiens (human) | 2720 | GLB1 |
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DOID:0080501 | GM1 gangliosidosis type 2 | HGNC:4298 | Homo sapiens (human) | 2720 | GLB1 |
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DOID:3322 | GM1 gangliosidosis | HGNC:4298 | Homo sapiens (human) | 2720 | GLB1 |
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DOID:0080489 | GM1 gangliosidosis type 3 | HGNC:4298 | Homo sapiens (human) | 2720 | GLB1 |
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DOID:14499 | Fabry disease | HGNC:4296 | Homo sapiens (human) | 2717 | GLA |
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DOID:3211 | lysosomal storage disease | HGNC:4296 | Homo sapiens (human) | 2717 | GLA |
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DOID:0060363 | glycerol kinase deficiency | HGNC:4291 | Homo sapiens (human) | 2712 | GK2 |
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DOID:0060363 | glycerol kinase deficiency | HGNC:4289 | Homo sapiens (human) | 2710 | GK |
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DOID:13810 | familial hypercholesterolemia | HGNC:4289 | Homo sapiens (human) | 2710 | GK |
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DOID:1574 | alcohol use disorder | SGD:S000000856 | Saccharomyces cerevisiae S288C | 856781 | GIP2 |
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DOID:9993 | hypoglycemia | SGD:S000000856 | Saccharomyces cerevisiae S288C | 856781 | GIP2 |
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DOID:9352 | type 2 diabetes mellitus | SGD:S000000856 | Saccharomyces cerevisiae S288C | 856781 | GIP2 |
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DOID:4914 | esophagus adenocarcinoma | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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DOID:9352 | type 2 diabetes mellitus | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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DOID:3125 | multiple endocrine neoplasia | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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DOID:11983 | Prader-Willi syndrome | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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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