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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:162 | cancer | HGNC:8907 | Homo sapiens (human) | 5238 | PGM3 |
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| DOID:2747 | glycogen storage disease | HGNC:8925 | Homo sapiens (human) | 5255 | PHKA1 |
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| DOID:1459 | hypothyroidism | HGNC:8925 | Homo sapiens (human) | 5255 | PHKA1 |
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| DOID:0111040 | glycogen storage disease IXd | HGNC:8925 | Homo sapiens (human) | 5255 | PHKA1 |
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| DOID:0050545 | visceral heterotaxy | HGNC:8926 | Homo sapiens (human) | 5256 | PHKA2 |
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| DOID:0111042 | glycogen storage disease IXa | HGNC:8926 | Homo sapiens (human) | 5256 | PHKA2 |
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| DOID:2747 | glycogen storage disease | HGNC:8926 | Homo sapiens (human) | 5256 | PHKA2 |
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| DOID:0111041 | glycogen storage disease IXb | HGNC:8927 | Homo sapiens (human) | 5257 | PHKB |
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| DOID:5082 | liver cirrhosis | HGNC:8931 | Homo sapiens (human) | 5261 | PHKG2 |
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| DOID:2747 | glycogen storage disease | HGNC:8931 | Homo sapiens (human) | 5261 | PHKG2 |
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| DOID:0111043 | glycogen storage disease IXc | HGNC:8931 | Homo sapiens (human) | 5261 | PHKG2 |
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| DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | HGNC:8957 | Homo sapiens (human) | 5277 | PIGA |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | HGNC:8957 | Homo sapiens (human) | 5277 | PIGA |
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| DOID:0060284 | paroxysmal nocturnal hemoglobinuria | HGNC:8957 | Homo sapiens (human) | 5277 | PIGA |
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| DOID:0112216 | developmental and epileptic encephalopathy 80 | HGNC:8959 | Homo sapiens (human) | 9488 | PIGB |
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| DOID:10112 | sleeping sickness | HGNC:8959 | Homo sapiens (human) | 9488 | PIGB |
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| DOID:0081223 | glycosylphosphatidylinositol biosynthesis defect 16 | HGNC:8960 | Homo sapiens (human) | 5279 | PIGC |
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| DOID:0112152 | CHIME syndrome | HGNC:8966 | Homo sapiens (human) | 9487 | PIGL |
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| DOID:0080138 | multiple congenital anomalies-hypotonia-seizures syndrome 1 | HGNC:8967 | Homo sapiens (human) | 23556 | PIGN |
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| DOID:4621 | holoprosencephaly | HGNC:8967 | Homo sapiens (human) | 23556 | PIGN |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:8971 | Homo sapiens (human) | 5286 | PIK3C2A |
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| DOID:83 | cataract | HGNC:8971 | Homo sapiens (human) | 5286 | PIK3C2A |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:8973 | Homo sapiens (human) | 5288 | PIK3C2G |
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| DOID:0050589 | inflammatory bowel disease | HGNC:8974 | Homo sapiens (human) | 5289 | PIK3C3 |
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| DOID:10534 | stomach cancer | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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