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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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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:224 | transient cerebral ischemia | RGD:2721 | Rattus norvegicus (Norway rat) | 24401 | Got1 |
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| DOID:9452 | steatotic liver disease | MGI:109354 | Mus musculus (house mouse) | 22228 | Ucp2 |
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| DOID:4450 | renal cell carcinoma | HGNC:8729 | Homo sapiens (human) | 5111 | PCNA |
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| DOID:11335 | sarcoidosis | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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| DOID:10024 | migraine with aura | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:0112223 | developmental and epileptic encephalopathy 89 | HGNC:4092 | Homo sapiens (human) | 2571 | GAD1 |
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| DOID:0110184 | Charcot-Marie-Tooth disease type 4J | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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| DOID:0111103 | maturity-onset diabetes of the young type 4 | RGD:62387 | Rattus norvegicus (Norway rat) | 29535 | Pdx1 |
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| DOID:0060576 | 3MC syndrome 2 | HGNC:17213 | Homo sapiens (human) | 78989 | COLEC11 |
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| DOID:10605 | short bowel syndrome | MGI:104993 | Mus musculus (house mouse) | 16847 | Lepr |
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| DOID:2957 | pulmonary tuberculosis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:9884 | muscular dystrophy | Xenbase:XB-GENE-6489079 | Xenopus laevis (African clawed frog) | 108698684 | pomt2.L |
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| DOID:583 | hemolytic anemia | Xenbase:XB-GENE-5962599 | Xenopus tropicalis (tropical clawed frog) | 549437 | abo.3 |
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| DOID:0050642 | hypochromic microcytic anemia | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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| DOID:783 | end stage renal disease | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:2367 | neuroaxonal dystrophy | HGNC:9039 | Homo sapiens (human) | 8398 | PLA2G6 |
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| DOID:10211 | cholelithiasis | HGNC:2593 | Homo sapiens (human) | 1586 | CYP17A1 |
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| DOID:784 | chronic kidney disease | HGNC:9922 | Homo sapiens (human) | 5950 | RBP4 |
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| DOID:3649 | pyruvate decarboxylase deficiency | HGNC:2896 | Homo sapiens (human) | 1737 | DLAT |
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| DOID:0080178 | mucositis | HGNC:8729 | Homo sapiens (human) | 5111 | PCNA |
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| DOID:2316 | brain ischemia | HGNC:8729 | Homo sapiens (human) | 5111 | PCNA |
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| DOID:1289 | neurodegenerative disease | SGD:S000004295 | Saccharomyces cerevisiae S288C | 851013 | ACO1 |
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| DOID:3525 | middle cerebral artery infarction | HGNC:6783 | Homo sapiens (human) | 4099 | MAG |
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| DOID:8515 | Cor pulmonale | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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| DOID:8725 | vascular dementia | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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