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:557 | kidney disease | MGI:102519 | Mus musculus (house mouse) | 13010 | Cst3 |
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DOID:10652 | Alzheimer's disease | MGI:102519 | Mus musculus (house mouse) | 13010 | Cst3 |
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DOID:9970 | obesity | MGI:102519 | Mus musculus (house mouse) | 13010 | Cst3 |
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DOID:6000 | congestive heart failure | MGI:102519 | Mus musculus (house mouse) | 13010 | Cst3 |
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DOID:1389 | polyneuropathy | MGI:102519 | Mus musculus (house mouse) | 13010 | Cst3 |
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DOID:11758 | iron deficiency anemia | MGI:102519 | Mus musculus (house mouse) | 13010 | Cst3 |
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DOID:2377 | multiple sclerosis | MGI:102519 | Mus musculus (house mouse) | 13010 | Cst3 |
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DOID:2316 | brain ischemia | MGI:102519 | Mus musculus (house mouse) | 13010 | Cst3 |
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DOID:10941 | intracranial aneurysm | MGI:102519 | Mus musculus (house mouse) | 13010 | Cst3 |
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DOID:10591 | pre-eclampsia | MGI:102519 | Mus musculus (house mouse) | 13010 | Cst3 |
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DOID:0070027 | CST3-related cerebral amyloid angiopathy | MGI:102519 | Mus musculus (house mouse) | 13010 | Cst3 |
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DOID:0110023 | age related macular degeneration 11 | MGI:102519 | Mus musculus (house mouse) | 13010 | Cst3 |
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DOID:12842 | Guillain-Barre syndrome | MGI:102519 | Mus musculus (house mouse) | 13010 | Cst3 |
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DOID:0050564 | autosomal dominant nonsyndromic deafness | HGNC:2186 | Homo sapiens (human) | 1301 | COL11A1 |
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DOID:0080672 | fibrochondrogenesis 1 | HGNC:2186 | Homo sapiens (human) | 1301 | COL11A1 |
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DOID:0111510 | Marshall syndrome | HGNC:2186 | Homo sapiens (human) | 1301 | COL11A1 |
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DOID:0080046 | Stickler syndrome | HGNC:2186 | Homo sapiens (human) | 1301 | COL11A1 |
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DOID:8398 | osteoarthritis | HGNC:2186 | Homo sapiens (human) | 1301 | COL11A1 |
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DOID:0080675 | Stickler syndrome 2 | HGNC:2186 | Homo sapiens (human) | 1301 | COL11A1 |
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DOID:5844 | myocardial infarction | MGI:102889 | Mus musculus (house mouse) | 13003 | Vcan |
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DOID:10941 | intracranial aneurysm | MGI:102889 | Mus musculus (house mouse) | 13003 | Vcan |
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DOID:12336 | male infertility | MGI:88547 | Mus musculus (house mouse) | 13000 | Csnk2a2 |
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DOID:0080021 | Schmid metaphyseal chondrodysplasia | HGNC:2185 | Homo sapiens (human) | 1300 | COL10A1 |
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DOID:90 | degenerative disc disease | HGNC:2185 | Homo sapiens (human) | 1300 | COL10A1 |
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DOID:3910 | lung adenocarcinoma | HGNC:2185 | Homo sapiens (human) | 1300 | COL10A1 |
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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