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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:9074 | systemic lupus erythematosus | HGNC:6079 | Homo sapiens (human) | 3635 | INPP5D |
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| DOID:9970 | obesity | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:5844 | myocardial infarction | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:2394 | ovarian cancer | HGNC:3148 | Homo sapiens (human) | 1890 | TYMP |
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| DOID:10283 | prostate cancer | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:5679 | retinal disease | HGNC:17852 | Homo sapiens (human) | 56994 | CHPT1 |
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| DOID:2043 | hepatitis B | HGNC:12538 | Homo sapiens (human) | 54578 | UGT1A6 |
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| DOID:3459 | breast carcinoma | HGNC:11285 | Homo sapiens (human) | 6716 | SRD5A2 |
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| DOID:11714 | gestational diabetes | HGNC:4250 | Homo sapiens (human) | 2678 | GGT1 |
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| DOID:13619 | extrahepatic cholestasis | HGNC:6561 | Homo sapiens (human) | 3956 | LGALS1 |
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| DOID:9719 | neovascular inflammatory vitreoretinopathy | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:1826 | epilepsy | HGNC:4141 | Homo sapiens (human) | 2597 | GAPDH |
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| DOID:0050644 | arterial calcification of infancy | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
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| DOID:2513 | basal cell carcinoma | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:11832 | visual epilepsy | HGNC:9067 | Homo sapiens (human) | 5337 | PLD1 |
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| DOID:3070 | high grade glioma | HGNC:10860 | Homo sapiens (human) | 6480 | ST6GAL1 |
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| DOID:1826 | epilepsy | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:13580 | cholestasis | HGNC:253 | Homo sapiens (human) | 128 | ADH5 |
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| DOID:10754 | otitis media | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:2581 | chondrodysplasia punctata | HGNC:10545 | Homo sapiens (human) | 6307 | MSMO1 |
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| DOID:4194 | glucose metabolism disease | HGNC:4923 | Homo sapiens (human) | 3099 | HK2 |
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| DOID:0050560 | Walker-Warburg syndrome | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:9111 | cutaneous leishmaniasis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:8689 | anorexia nervosa | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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| DOID:2394 | ovarian cancer | HGNC:2594 | Homo sapiens (human) | 1588 | CYP19A1 |
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