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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:0111458 | galactose epimerase deficiency | HGNC:4116 | Homo sapiens (human) | 2582 | GALE |
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| DOID:0110777 | hereditary spastic paraplegia 26 | HGNC:4117 | Homo sapiens (human) | 2583 | B4GALNT1 |
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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: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:4079 | heart valve disease | HGNC:4123 | Homo sapiens (human) | 2589 | GALNT1 |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:4124 | Homo sapiens (human) | 2590 | GALNT2 |
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| DOID:0111063 | hyperphosphatemic familial tumoral calcinosis | HGNC:4125 | Homo sapiens (human) | 2591 | GALNT3 |
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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: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:9970 | obesity | HGNC:4141 | Homo sapiens (human) | 2597 | GAPDH |
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| DOID:10652 | Alzheimer's disease | HGNC:4141 | Homo sapiens (human) | 2597 | GAPDH |
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| DOID:0060108 | brain glioma | HGNC:4141 | Homo sapiens (human) | 2597 | GAPDH |
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| DOID:3319 | lymphangioleiomyomatosis | HGNC:4141 | Homo sapiens (human) | 2597 | GAPDH |
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| DOID:3525 | middle cerebral artery infarction | HGNC:4141 | Homo sapiens (human) | 2597 | GAPDH |
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| 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:9869 | hereditary fructose intolerance syndrome | HGNC:417 | Homo sapiens (human) | 229 | ALDOB |
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| DOID:916 | liver benign neoplasm | HGNC:417 | Homo sapiens (human) | 229 | ALDOB |
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