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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:11714 | gestational diabetes | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:13317 | hyperinsulinemic hypoglycemia | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:9351 | diabetes mellitus | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:0111100 | maturity-onset diabetes of the young type 2 | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:0070216 | familial hyperinsulinemic hypoglycemia 3 | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:10763 | hypertension | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:2018 | hyperinsulinism | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:3393 | coronary artery disease | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:0060639 | permanent neonatal diabetes mellitus | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:9452 | steatotic liver disease | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:4195 | hyperglycemia | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:0050524 | maturity-onset diabetes of the young | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:4194 | glucose metabolism disease | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:9970 | obesity | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:9993 | hypoglycemia | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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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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| DOID:0111254 | glutaric acidemia I | HGNC:4189 | Homo sapiens (human) | 2639 | GCDH |
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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:557 | kidney disease | HGNC:19069 | Homo sapiens (human) | 57733 | GBA3 |
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| DOID:0110798 | hereditary spastic paraplegia 46 | HGNC:18986 | Homo sapiens (human) | 57704 | GBA2 |
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| DOID:0050474 | Netherton syndrome | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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