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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:2018 | hyperinsulinism | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:1824 | status epilepticus | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:0080855 | Parkinsonism | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:0111110 | maturity-onset diabetes of the young type 13 | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:0080572 | congenital disorder of glycosylation Iw | HGNC:6172 | Homo sapiens (human) | 3703 | STT3A |
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| DOID:10914 | amnestic disorder | HGNC:6126 | Homo sapiens (human) | 8660 | IRS2 |
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| DOID:4194 | glucose metabolism disease | HGNC:6126 | Homo sapiens (human) | 8660 | IRS2 |
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| DOID:1059 | intellectual disability | HGNC:6126 | Homo sapiens (human) | 8660 | IRS2 |
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| DOID:11476 | osteoporosis | HGNC:6126 | Homo sapiens (human) | 8660 | IRS2 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:6126 | Homo sapiens (human) | 8660 | IRS2 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:6126 | Homo sapiens (human) | 8660 | IRS2 |
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| DOID:10652 | Alzheimer's disease | HGNC:6126 | Homo sapiens (human) | 8660 | IRS2 |
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| DOID:10652 | Alzheimer's disease | HGNC:612 | Homo sapiens (human) | 347 | APOD |
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| DOID:11714 | gestational diabetes | HGNC:612 | Homo sapiens (human) | 347 | APOD |
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| DOID:1824 | status epilepticus | HGNC:612 | Homo sapiens (human) | 347 | APOD |
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| DOID:4762 | vasculogenic impotence | HGNC:612 | Homo sapiens (human) | 347 | APOD |
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| DOID:9970 | obesity | HGNC:612 | Homo sapiens (human) | 347 | APOD |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:612 | Homo sapiens (human) | 347 | APOD |
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| DOID:9351 | diabetes mellitus | HGNC:6107 | Homo sapiens (human) | 3651 | PDX1 |
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| DOID:3526 | cerebral infarction | HGNC:6107 | Homo sapiens (human) | 3651 | PDX1 |
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| DOID:9970 | obesity | HGNC:6107 | Homo sapiens (human) | 3651 | PDX1 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:6107 | Homo sapiens (human) | 3651 | PDX1 |
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| DOID:0050524 | maturity-onset diabetes of the young | HGNC:6107 | Homo sapiens (human) | 3651 | PDX1 |
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| DOID:0080998 | acute necrotizing pancreatitis | HGNC:6107 | Homo sapiens (human) | 3651 | PDX1 |
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| DOID:3891 | placental insufficiency | HGNC:6107 | Homo sapiens (human) | 3651 | PDX1 |
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