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:12351 | alcoholic hepatitis | MGI:99216 | Mus musculus (house mouse) | 12305 | Ddr1 |
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DOID:3347 | osteosarcoma | MGI:99216 | Mus musculus (house mouse) | 12305 | Ddr1 |
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DOID:3908 | lung non-small cell carcinoma | MGI:99216 | Mus musculus (house mouse) | 12305 | Ddr1 |
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DOID:1612 | breast cancer | MGI:99216 | Mus musculus (house mouse) | 12305 | Ddr1 |
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DOID:684 | hepatocellular carcinoma | MGI:99216 | Mus musculus (house mouse) | 12305 | Ddr1 |
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DOID:10123 | pigmentation disease | HGNC:10978 | Homo sapiens (human) | 123041 | SLC24A4 |
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DOID:0110063 | amelogenesis imperfecta hypomaturation type 2A5 | HGNC:10978 | Homo sapiens (human) | 123041 | SLC24A4 |
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DOID:1826 | epilepsy | HGNC:10978 | Homo sapiens (human) | 123041 | SLC24A4 |
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DOID:0110398 | retinitis pigmentosa 51 | HGNC:20087 | Homo sapiens (human) | 123016 | TTC8 |
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DOID:0110130 | Bardet-Biedl syndrome 8 | HGNC:20087 | Homo sapiens (human) | 123016 | TTC8 |
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DOID:0060340 | ciliopathy | HGNC:20087 | Homo sapiens (human) | 123016 | TTC8 |
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DOID:1935 | Bardet-Biedl syndrome | HGNC:20087 | Homo sapiens (human) | 123016 | TTC8 |
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DOID:1793 | pancreatic cancer | MGI:1270839 | Mus musculus (house mouse) | 12301 | Cacybp |
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DOID:5844 | myocardial infarction | MGI:1270839 | Mus musculus (house mouse) | 12301 | Cacybp |
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DOID:0070040 | autosomal dominant intellectual developmental disorder 10 | MGI:1316660 | Mus musculus (house mouse) | 12300 | Cacng2 |
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DOID:1825 | childhood absence epilepsy | MGI:1316660 | Mus musculus (house mouse) | 12300 | Cacng2 |
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DOID:1407 | anterior uveitis | HGNC:1602 | Homo sapiens (human) | 1230 | CCR1 |
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DOID:12217 | Lewy body dementia | HGNC:1602 | Homo sapiens (human) | 1230 | CCR1 |
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DOID:9246 | cerebral amyloid angiopathy | HGNC:1602 | Homo sapiens (human) | 1230 | CCR1 |
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DOID:3042 | allergic contact dermatitis | HGNC:1602 | Homo sapiens (human) | 1230 | CCR1 |
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DOID:5082 | liver cirrhosis | HGNC:1602 | Homo sapiens (human) | 1230 | CCR1 |
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DOID:10652 | Alzheimer's disease | HGNC:1602 | Homo sapiens (human) | 1230 | CCR1 |
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DOID:0080599 | Coronavirus infectious disease | HGNC:1602 | Homo sapiens (human) | 1230 | CCR1 |
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DOID:3393 | coronary artery disease | HGNC:1602 | Homo sapiens (human) | 1230 | CCR1 |
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DOID:0060180 | colitis | HGNC:1602 | Homo sapiens (human) | 1230 | CCR1 |
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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