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:0080855 | Parkinsonism | HGNC:11917 | Homo sapiens (human) | 7133 | TNFRSF1B |
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DOID:6000 | congestive heart failure | HGNC:11917 | Homo sapiens (human) | 7133 | TNFRSF1B |
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DOID:7147 | ankylosing spondylitis | HGNC:11917 | Homo sapiens (human) | 7133 | TNFRSF1B |
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DOID:5199 | ureteral obstruction | HGNC:11917 | Homo sapiens (human) | 7133 | TNFRSF1B |
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DOID:0080162 | lupus nephritis | HGNC:11916 | Homo sapiens (human) | 7132 | TNFRSF1A |
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DOID:841 | extrinsic allergic alveolitis | HGNC:11916 | Homo sapiens (human) | 7132 | TNFRSF1A |
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DOID:13141 | uveitis | HGNC:11916 | Homo sapiens (human) | 7132 | TNFRSF1A |
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DOID:2316 | brain ischemia | HGNC:11916 | Homo sapiens (human) | 7132 | TNFRSF1A |
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DOID:0050848 | obstructive sleep apnea | HGNC:11916 | Homo sapiens (human) | 7132 | TNFRSF1A |
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DOID:0050157 | cryptogenic organizing pneumonia | HGNC:11916 | Homo sapiens (human) | 7132 | TNFRSF1A |
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DOID:8893 | psoriasis | HGNC:11916 | Homo sapiens (human) | 7132 | TNFRSF1A |
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DOID:0090018 | autosomal dominant familial periodic fever | HGNC:11916 | Homo sapiens (human) | 7132 | TNFRSF1A |
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DOID:5199 | ureteral obstruction | HGNC:11916 | Homo sapiens (human) | 7132 | TNFRSF1A |
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DOID:5844 | myocardial infarction | HGNC:11916 | Homo sapiens (human) | 7132 | TNFRSF1A |
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DOID:557 | kidney disease | HGNC:11916 | Homo sapiens (human) | 7132 | TNFRSF1A |
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DOID:9352 | type 2 diabetes mellitus | HGNC:11916 | Homo sapiens (human) | 7132 | TNFRSF1A |
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DOID:9074 | systemic lupus erythematosus | HGNC:11916 | Homo sapiens (human) | 7132 | TNFRSF1A |
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DOID:13166 | allergic bronchopulmonary aspergillosis | HGNC:11916 | Homo sapiens (human) | 7132 | TNFRSF1A |
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DOID:2355 | anemia | HGNC:11916 | Homo sapiens (human) | 7132 | TNFRSF1A |
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DOID:2377 | multiple sclerosis | HGNC:11916 | Homo sapiens (human) | 7132 | TNFRSF1A |
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DOID:6543 | acne | HGNC:11916 | Homo sapiens (human) | 7132 | TNFRSF1A |
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DOID:4450 | renal cell carcinoma | HGNC:11916 | Homo sapiens (human) | 7132 | TNFRSF1A |
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DOID:224 | transient cerebral ischemia | HGNC:11916 | Homo sapiens (human) | 7132 | TNFRSF1A |
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DOID:326 | ischemia | HGNC:11916 | Homo sapiens (human) | 7132 | TNFRSF1A |
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DOID:8778 | Crohn's disease | HGNC:11916 | Homo sapiens (human) | 7132 | TNFRSF1A |
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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