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:83 | cataract | MGI:104990 | Mus musculus (house mouse) | 14629 | Gclc |
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DOID:5082 | liver cirrhosis | MGI:104990 | Mus musculus (house mouse) | 14629 | Gclc |
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DOID:9256 | colorectal cancer | MGI:104990 | Mus musculus (house mouse) | 14629 | Gclc |
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DOID:583 | hemolytic anemia | MGI:104990 | Mus musculus (house mouse) | 14629 | Gclc |
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DOID:0111681 | glutamate-cysteine ligase deficiency | MGI:104990 | Mus musculus (house mouse) | 14629 | Gclc |
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DOID:83 | cataract | MGI:95730 | Mus musculus (house mouse) | 14635 | Galk1 |
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DOID:14695 | galactokinase deficiency | MGI:95730 | Mus musculus (house mouse) | 14635 | Galk1 |
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DOID:2316 | brain ischemia | HGNC:2466 | Homo sapiens (human) | 1464 | CSPG4 |
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DOID:2378 | relapsing-remitting multiple sclerosis | HGNC:2466 | Homo sapiens (human) | 1464 | CSPG4 |
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DOID:9952 | acute lymphoblastic leukemia | HGNC:2466 | Homo sapiens (human) | 1464 | CSPG4 |
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DOID:4795 | GM2 gangliosidosis, AB variant | MGI:95762 | Mus musculus (house mouse) | 14667 | Gm2a |
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DOID:3321 | GM2 gangliosidosis | MGI:95762 | Mus musculus (house mouse) | 14667 | Gm2a |
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DOID:0070450 | mitochondrial DNA depletion syndrome 19 | HGNC:10980 | Homo sapiens (human) | 1468 | SLC25A10 |
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DOID:0070329 | mitochondrial DNA depletion syndrome | HGNC:10980 | Homo sapiens (human) | 1468 | SLC25A10 |
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DOID:0060536 | mitochondrial complex I deficiency | HGNC:10980 | Homo sapiens (human) | 1468 | SLC25A10 |
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DOID:0060475 | myoclonic-atonic epilepsy | HGNC:10980 | Homo sapiens (human) | 1468 | SLC25A10 |
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DOID:0070268 | congenital disorder of glycosylation type IIp | HGNC:18085 | Homo sapiens (human) | 147007 | TMEM199 |
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DOID:684 | hepatocellular carcinoma | MGI:1202304 | Mus musculus (house mouse) | 14711 | Gnmt |
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DOID:0111037 | glycine N-methyltransferase deficiency | MGI:1202304 | Mus musculus (house mouse) | 14711 | Gnmt |
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DOID:9120 | amyloidosis | MGI:95791 | Mus musculus (house mouse) | 14718 | Got1 |
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DOID:0050700 | cardiomyopathy | MGI:95791 | Mus musculus (house mouse) | 14718 | Got1 |
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DOID:332 | amyotrophic lateral sclerosis | MGI:95791 | Mus musculus (house mouse) | 14718 | Got1 |
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DOID:224 | transient cerebral ischemia | MGI:95791 | Mus musculus (house mouse) | 14718 | Got1 |
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DOID:3498 | pancreatic ductal adenocarcinoma | MGI:95791 | Mus musculus (house mouse) | 14718 | Got1 |
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DOID:9952 | acute lymphoblastic leukemia | MGI:95797 | Mus musculus (house mouse) | 14751 | Gpi1 |
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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