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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:3651 | pyruvate carboxylase deficiency disease | HGNC:8636 | Homo sapiens (human) | 5091 | PC |
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| DOID:10003 | sensorineural hearing loss | HGNC:11720 | Homo sapiens (human) | 7007 | TECTA |
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| DOID:11396 | pulmonary edema | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:2018 | hyperinsulinism | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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| DOID:1926 | Gaucher's disease | HGNC:9020 | Homo sapiens (human) | 5313 | PKLR |
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| DOID:655 | inherited metabolic disorder | HGNC:5209 | Homo sapiens (human) | 3291 | HSD11B2 |
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| DOID:2747 | glycogen storage disease | HGNC:4707 | Homo sapiens (human) | 2998 | GYS2 |
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| DOID:3146 | lipid metabolism disorder | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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| DOID:11151 | cholecystolithiasis | HGNC:9031 | Homo sapiens (human) | 5320 | PLA2G2A |
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| DOID:0080217 | lysosomal acid lipase deficiency | MGI:96789 | Mus musculus (house mouse) | 16889 | Lipa |
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| DOID:1612 | breast cancer | HGNC:9065 | Homo sapiens (human) | 5335 | PLCG1 |
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| DOID:2018 | hyperinsulinism | RGD:3307 | Rattus norvegicus (Norway rat) | 24638 | Pfkfb1 |
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| DOID:8567 | Hodgkin's lymphoma | HGNC:10658 | Homo sapiens (human) | 6382 | SDC1 |
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| DOID:10652 | Alzheimer's disease | HGNC:612 | Homo sapiens (human) | 347 | APOD |
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| DOID:5844 | myocardial infarction | RGD:619719 | Rattus norvegicus (Norway rat) | 81829 | Mdh2 |
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| DOID:224 | transient cerebral ischemia | RGD:3269 | Rattus norvegicus (Norway rat) | 25737 | Pcna |
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| DOID:1909 | melanoma | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:891 | progressive myoclonus epilepsy | HGNC:3413 | Homo sapiens (human) | 7957 | EPM2A |
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| DOID:9993 | hypoglycemia | HGNC:9291 | Homo sapiens (human) | 5506 | PPP1R3A |
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| DOID:9744 | type 1 diabetes mellitus | RGD:3935 | Rattus norvegicus (Norway rat) | 24861 | Ugt1a1 |
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| DOID:2986 | IgA glomerulonephritis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0050426 | Stevens-Johnson syndrome | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:3049 | Churg-Strauss syndrome | HGNC:4243 | Homo sapiens (human) | 2674 | GFRA1 |
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| DOID:9810 | polyarteritis nodosa | HGNC:4243 | Homo sapiens (human) | 2674 | GFRA1 |
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| DOID:0080379 | nephrotic syndrome type 2 | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
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