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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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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID ▼ | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:11446 | sciatic neuropathy | HGNC:29595 | Homo sapiens (human) | 130120 | REG3G |
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| DOID:11832 | visual epilepsy | HGNC:29595 | Homo sapiens (human) | 130120 | REG3G |
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| DOID:552 | pneumonia | HGNC:29595 | Homo sapiens (human) | 130120 | REG3G |
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| DOID:2913 | acute pancreatitis | HGNC:29595 | Homo sapiens (human) | 130120 | REG3G |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:29595 | Homo sapiens (human) | 130120 | REG3G |
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| DOID:2256 | osteochondrodysplasia | HGNC:2218 | Homo sapiens (human) | 1298 | COL9A2 |
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| DOID:0080046 | Stickler syndrome | HGNC:2218 | Homo sapiens (human) | 1298 | COL9A2 |
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| DOID:0070298 | multiple epiphyseal dysplasia 2 | HGNC:2218 | Homo sapiens (human) | 1298 | COL9A2 |
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| DOID:3312 | bipolar disorder | MGI:88529 | Mus musculus (house mouse) | 12974 | Cs |
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| DOID:8466 | retinal degeneration | MGI:88529 | Mus musculus (house mouse) | 12974 | Cs |
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| DOID:0050852 | limb ischemia | MGI:88529 | Mus musculus (house mouse) | 12974 | Cs |
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| DOID:11984 | hypertrophic cardiomyopathy | MGI:88529 | Mus musculus (house mouse) | 12974 | Cs |
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| DOID:12930 | dilated cardiomyopathy | MGI:88529 | Mus musculus (house mouse) | 12974 | Cs |
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| DOID:5844 | myocardial infarction | MGI:88529 | Mus musculus (house mouse) | 12974 | Cs |
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| DOID:7998 | hyperthyroidism | MGI:88529 | Mus musculus (house mouse) | 12974 | Cs |
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| DOID:6000 | congestive heart failure | MGI:88529 | Mus musculus (house mouse) | 12974 | Cs |
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| DOID:1459 | hypothyroidism | MGI:88529 | Mus musculus (house mouse) | 12974 | Cs |
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| DOID:0111141 | delayed sleep phase syndrome | MGI:1270841 | Mus musculus (house mouse) | 12952 | Cry1 |
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| DOID:0050558 | Ullrich congenital muscular dystrophy | HGNC:2211 | Homo sapiens (human) | 1291 | COL6A1 |
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| DOID:0050663 | Bethlem myopathy | HGNC:2211 | Homo sapiens (human) | 1291 | COL6A1 |
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| DOID:9884 | muscular dystrophy | HGNC:2211 | Homo sapiens (human) | 1291 | COL6A1 |
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| DOID:0050557 | congenital muscular dystrophy | HGNC:2211 | Homo sapiens (human) | 1291 | COL6A1 |
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| DOID:783 | end stage renal disease | MGI:1098296 | Mus musculus (house mouse) | 12894 | Cpt1a |
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| DOID:3146 | lipid metabolism disorder | MGI:1098296 | Mus musculus (house mouse) | 12894 | Cpt1a |
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| DOID:3319 | lymphangioleiomyomatosis | MGI:1098296 | Mus musculus (house mouse) | 12894 | Cpt1a |
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