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Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
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Repository for lectin-assisted multimodality data
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Alliance of Genome Resources
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 |
|---|---|
| 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 |
|---|---|---|---|---|---|---|---|---|
| DOID:9352 | type 2 diabetes mellitus | MGI:107189 | Mus musculus (house mouse) | 11625 | Ahsg |
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| DOID:5844 | myocardial infarction | MGI:107189 | Mus musculus (house mouse) | 11625 | Ahsg |
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| DOID:11714 | gestational diabetes | MGI:107189 | Mus musculus (house mouse) | 11625 | Ahsg |
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| DOID:3393 | coronary artery disease | MGI:107189 | Mus musculus (house mouse) | 11625 | Ahsg |
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| DOID:9970 | obesity | MGI:107189 | Mus musculus (house mouse) | 11625 | Ahsg |
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| DOID:1826 | epilepsy | HGNC:21042 | Homo sapiens (human) | 116150 | NUS1 |
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| DOID:0080227 | autosomal dominant intellectual developmental disorder 55 | HGNC:21042 | Homo sapiens (human) | 116150 | NUS1 |
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| DOID:14330 | Parkinson's disease | HGNC:21042 | Homo sapiens (human) | 116150 | NUS1 |
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| DOID:0080553 | congenital disorder of glycosylation Iaa | HGNC:21042 | Homo sapiens (human) | 116150 | NUS1 |
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| DOID:5212 | congenital disorder of glycosylation | HGNC:21042 | Homo sapiens (human) | 116150 | NUS1 |
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| DOID:0111039 | hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | MGI:3643647 | Mus musculus (house mouse) | 11615 | Ahcyl |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | MGI:3643647 | Mus musculus (house mouse) | 11615 | Ahcyl |
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| DOID:7693 | abdominal aortic aneurysm | MGI:3643647 | Mus musculus (house mouse) | 11615 | Ahcyl |
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| DOID:8455 | pyridoxine deficiency anemia | MGI:3643647 | Mus musculus (house mouse) | 11615 | Ahcyl |
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| DOID:9452 | steatotic liver disease | MGI:3643647 | Mus musculus (house mouse) | 11615 | Ahcyl |
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| DOID:9279 | hyperhomocysteinemia | MGI:3643647 | Mus musculus (house mouse) | 11615 | Ahcyl |
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| DOID:6000 | congestive heart failure | HGNC:20842 | Homo sapiens (human) | 116113 | FOXP4 |
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| DOID:0060038 | specific developmental disorder | HGNC:20842 | Homo sapiens (human) | 116113 | FOXP4 |
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| DOID:3827 | congenital diaphragmatic hernia | MGI:87966 | Mus musculus (house mouse) | 11609 | Agtr2 |
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| DOID:1793 | pancreatic cancer | MGI:87966 | Mus musculus (house mouse) | 11609 | Agtr2 |
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| DOID:4450 | renal cell carcinoma | MGI:87966 | Mus musculus (house mouse) | 11609 | Agtr2 |
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| DOID:12930 | dilated cardiomyopathy | MGI:87966 | Mus musculus (house mouse) | 11609 | Agtr2 |
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| DOID:783 | end stage renal disease | MGI:87966 | Mus musculus (house mouse) | 11609 | Agtr2 |
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| DOID:2841 | asthma | MGI:87966 | Mus musculus (house mouse) | 11609 | Agtr2 |
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| DOID:10763 | hypertension | MGI:87966 | Mus musculus (house mouse) | 11609 | Agtr2 |
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