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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:9352 | type 2 diabetes mellitus | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:263 | kidney cancer | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:10652 | Alzheimer's disease | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:11446 | sciatic neuropathy | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:12236 | primary biliary cholangitis | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:0050328 | congenital hypothyroidism | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:0060180 | colitis | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:12930 | dilated cardiomyopathy | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:14330 | Parkinson's disease | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:3891 | placental insufficiency | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:1074 | kidney failure | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:12858 | Huntington's disease | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:11716 | prediabetes syndrome | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:1909 | melanoma | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:4448 | macular degeneration | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:1184 | nephrotic syndrome | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:1907 | malignant fibrous histiocytoma | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:7998 | hyperthyroidism | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:10871 | age related macular degeneration | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:8947 | diabetic retinopathy | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:9452 | steatotic liver disease | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:0050753 | cerebellar ataxia | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:2476 | hereditary spastic paraplegia | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:0110790 | hereditary spastic paraplegia 39 | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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