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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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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References ▲ |
|---|---|---|---|---|---|---|---|---|
| DOID:12241 | beta thalassemia | HGNC:5472 | Homo sapiens (human) | 3486 | IGFBP3 |
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| DOID:2018 | hyperinsulinism | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:6709 | Homo sapiens (human) | 4049 | LTA |
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| DOID:2316 | brain ischemia | RGD:620596 | Rattus norvegicus (Norway rat) | 117029 | Ccr5 |
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| DOID:11832 | visual epilepsy | RGD:3633 | Rattus norvegicus (Norway rat) | 25349 | Scn2b |
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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:8501 | fundus dystrophy | HGNC:9942 | Homo sapiens (human) | 5961 | PRPH2 |
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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:3407 | carotid artery disease | HGNC:2545 | Homo sapiens (human) | 1520 | CTSS |
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| DOID:10003 | sensorineural hearing loss | HGNC:6001 | Homo sapiens (human) | 3558 | IL2 |
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| DOID:655 | inherited metabolic disorder | HGNC:983 | Homo sapiens (human) | 590 | BCHE |
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| DOID:2228 | thrombocytosis | HGNC:11795 | Homo sapiens (human) | 7066 | THPO |
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| DOID:11151 | cholecystolithiasis | HGNC:9031 | Homo sapiens (human) | 5320 | PLA2G2A |
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| DOID:1394 | urinary schistosomiasis | HGNC:6016 | Homo sapiens (human) | 3567 | IL5 |
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| DOID:3627 | aortic aneurysm | RGD:3249 | Rattus norvegicus (Norway rat) | 24617 | Serpine1 |
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| DOID:13810 | familial hypercholesterolemia | HGNC:600 | Homo sapiens (human) | 335 | APOA1 |
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| DOID:2043 | hepatitis B | HGNC:1693 | Homo sapiens (human) | 968 | CD68 |
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| DOID:0080217 | lysosomal acid lipase deficiency | MGI:96789 | Mus musculus (house mouse) | 16889 | Lipa |
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| DOID:10652 | Alzheimer's disease | HGNC:8614 | Homo sapiens (human) | 5074 | PAWR |
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| DOID:9744 | type 1 diabetes mellitus | MGI:96556 | Mus musculus (house mouse) | 16189 | Il4 |
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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:1793 | pancreatic cancer | HGNC:173 | Homo sapiens (human) | 92 | ACVR2A |
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