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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:162 | cancer | FB:FBgn0266438 | Drosophila melanogaster (fruit fly) | 19835548 | PIG-Z |
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| DOID:9352 | type 2 diabetes mellitus | SGD:S000004263 | Saccharomyces cerevisiae S288C | 850979 | PIG1 |
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| DOID:1574 | alcohol use disorder | SGD:S000004263 | Saccharomyces cerevisiae S288C | 850979 | PIG1 |
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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:0070434 | hyperphosphatasia with impaired intellectual development syndrome 2 | HGNC:23215 | Homo sapiens (human) | 84720 | PIGO |
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| DOID:0080283 | developmental and epileptic encephalopathy 55 | HGNC:3046 | Homo sapiens (human) | 51227 | PIGP |
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| DOID:0112213 | multiple congenital anomalies-hypotonia-seizures syndrome 4 | HGNC:14135 | Homo sapiens (human) | 9091 | PIGQ |
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| DOID:0070382 | developmental and epileptic encephalopathy 95 | HGNC:14937 | Homo sapiens (human) | 94005 | PIGS |
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| DOID:0080140 | multiple congenital anomalies-hypotonia-seizures syndrome 3 | HGNC:14938 | Homo sapiens (human) | 51604 | PIGT |
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| DOID:0060284 | paroxysmal nocturnal hemoglobinuria | HGNC:14938 | Homo sapiens (human) | 51604 | PIGT |
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| DOID:0070433 | hyperphosphatasia with impaired intellectual development syndrome 1 | HGNC:26031 | Homo sapiens (human) | 55650 | PIGV |
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| DOID:0070432 | hyperphosphatasia with impaired intellectual development syndrome 5 | HGNC:23213 | Homo sapiens (human) | 284098 | PIGW |
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| DOID:0070437 | hyperphosphatasia with impaired intellectual development syndrome 6 | HGNC:28213 | Homo sapiens (human) | 84992 | PIGY |
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| DOID:162 | cancer | HGNC:30596 | Homo sapiens (human) | 80235 | PIGZ |
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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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