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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:0050827 | rheumatic heart disease | HGNC:4141 | Homo sapiens (human) | 2597 | GAPDH |
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| DOID:8947 | diabetic retinopathy | HGNC:4141 | Homo sapiens (human) | 2597 | GAPDH |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:4141 | Homo sapiens (human) | 2597 | GAPDH |
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| DOID:1826 | epilepsy | HGNC:4141 | Homo sapiens (human) | 2597 | GAPDH |
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| DOID:10652 | Alzheimer's disease | HGNC:24864 | Homo sapiens (human) | 26330 | GAPDHS |
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| DOID:0050474 | Netherton syndrome | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:8893 | psoriasis | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:0112250 | Gaucher's disease type IIIC | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:0110960 | Gaucher's disease perinatal lethal | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:0080855 | Parkinsonism | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:12217 | Lewy body dementia | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:0060892 | late onset Parkinson's disease | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:0110957 | Gaucher's disease type I | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:0110958 | Gaucher's disease type II | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:14330 | Parkinson's disease | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:0110959 | Gaucher's disease type III | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:1926 | Gaucher's disease | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:0110798 | hereditary spastic paraplegia 46 | HGNC:18986 | Homo sapiens (human) | 57704 | GBA2 |
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| DOID:557 | kidney disease | HGNC:19069 | Homo sapiens (human) | 57733 | GBA3 |
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| DOID:2750 | glycogen storage disease IV | HGNC:4180 | Homo sapiens (human) | 2632 | GBE1 |
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| DOID:2957 | pulmonary tuberculosis | HGNC:4180 | Homo sapiens (human) | 2632 | GBE1 |
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| DOID:13268 | porphyria | HGNC:4180 | Homo sapiens (human) | 2632 | GBE1 |
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| DOID:0111254 | glutaric acidemia I | HGNC:4189 | Homo sapiens (human) | 2639 | GCDH |
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| DOID:10652 | Alzheimer's disease | HGNC:4191 | Homo sapiens (human) | 2641 | GCG |
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| DOID:11716 | prediabetes syndrome | HGNC:4191 | Homo sapiens (human) | 2641 | GCG |
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