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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: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:0080322 | polycystic kidney disease | HGNC:4138 | Homo sapiens (human) | 23193 | GANAB |
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| DOID:0050770 | polycystic liver disease | HGNC:4138 | Homo sapiens (human) | 23193 | GANAB |
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| DOID:0110860 | polycystic kidney disease 3 | HGNC:4138 | Homo sapiens (human) | 23193 | GANAB |
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| DOID:9870 | galactosemia | HGNC:4135 | Homo sapiens (human) | 2592 | GALT |
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| DOID:0111459 | classic galactosemia | HGNC:4135 | Homo sapiens (human) | 2592 | GALT |
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| DOID:0111063 | hyperphosphatemic familial tumoral calcinosis | HGNC:4125 | Homo sapiens (human) | 2591 | GALNT3 |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:4124 | Homo sapiens (human) | 2590 | GALNT2 |
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| DOID:4079 | heart valve disease | HGNC:4123 | Homo sapiens (human) | 2589 | GALNT1 |
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| DOID:12804 | mucopolysaccharidosis IV | HGNC:4122 | Homo sapiens (human) | 2588 | GALNS |
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| DOID:0111391 | mucopolysaccharidosis IVA | HGNC:4122 | Homo sapiens (human) | 2588 | GALNS |
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| DOID:83 | cataract | HGNC:4118 | Homo sapiens (human) | 2584 | GALK1 |
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| DOID:14695 | galactokinase deficiency | HGNC:4118 | Homo sapiens (human) | 2584 | GALK1 |
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| DOID:0110777 | hereditary spastic paraplegia 26 | HGNC:4117 | Homo sapiens (human) | 2583 | B4GALNT1 |
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| DOID:1588 | thrombocytopenia | HGNC:4116 | Homo sapiens (human) | 2582 | GALE |
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| DOID:9870 | galactosemia | HGNC:4116 | Homo sapiens (human) | 2582 | GALE |
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| DOID:0111458 | galactose epimerase deficiency | HGNC:4116 | Homo sapiens (human) | 2582 | GALE |
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| DOID:13276 | Mycoplasma pneumoniae pneumonia | HGNC:4115 | Homo sapiens (human) | 2581 | GALC |
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| DOID:10587 | Krabbe disease | HGNC:4115 | Homo sapiens (human) | 2581 | GALC |
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| DOID:1909 | melanoma | HGNC:4115 | Homo sapiens (human) | 2581 | GALC |
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| DOID:11949 | Creutzfeldt-Jakob disease | HGNC:4115 | Homo sapiens (human) | 2581 | GALC |
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| DOID:14501 | Sjogren-Larsson syndrome | HGNC:411 | Homo sapiens (human) | 222 | ALDH3B2 |
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| DOID:14501 | Sjogren-Larsson syndrome | HGNC:410 | Homo sapiens (human) | 221 | ALDH3B1 |
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| DOID:1574 | alcohol use disorder | HGNC:4093 | Homo sapiens (human) | 2572 | GAD2 |
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