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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:4362 | cervical cancer | HGNC:8907 | Homo sapiens (human) | 5238 | PGM3 |
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| DOID:3307 | teratoma | HGNC:8907 | Homo sapiens (human) | 5238 | PGM3 |
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| DOID:0111953 | immunodeficiency 23 | HGNC:8907 | Homo sapiens (human) | 5238 | PGM3 |
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| DOID:162 | cancer | HGNC:8907 | Homo sapiens (human) | 5238 | PGM3 |
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| DOID:1380 | endometrial cancer | HGNC:8905 | Homo sapiens (human) | 5236 | PGM1 |
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| DOID:3307 | teratoma | HGNC:8905 | Homo sapiens (human) | 5236 | PGM1 |
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| DOID:0080570 | congenital disorder of glycosylation It | HGNC:8905 | Homo sapiens (human) | 5236 | PGM1 |
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| DOID:14330 | Parkinson's disease | HGNC:8898 | Homo sapiens (human) | 5232 | PGK2 |
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| DOID:162 | cancer | HGNC:8898 | Homo sapiens (human) | 5232 | PGK2 |
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| DOID:0111933 | phosphoglycerate kinase 1 deficiency | HGNC:8896 | Homo sapiens (human) | 5230 | PGK1 |
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| DOID:162 | cancer | HGNC:8896 | Homo sapiens (human) | 5230 | PGK1 |
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| DOID:583 | hemolytic anemia | HGNC:8896 | Homo sapiens (human) | 5230 | PGK1 |
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| DOID:14330 | Parkinson's disease | HGNC:8896 | Homo sapiens (human) | 5230 | PGK1 |
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| DOID:0112275 | developmental and epileptic encephalopathy 93 | HGNC:851 | Homo sapiens (human) | 523 | ATP6V1A |
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| DOID:0070129 | autosomal recessive cutis laxa type IID | HGNC:851 | Homo sapiens (human) | 523 | ATP6V1A |
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| DOID:0080108 | myoglobinuria | HGNC:8889 | Homo sapiens (human) | 5224 | PGAM2 |
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| DOID:2747 | glycogen storage disease | HGNC:8878 | Homo sapiens (human) | 5214 | PFKP |
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| DOID:0014667 | disease of metabolism | HGNC:8878 | Homo sapiens (human) | 5214 | PFKP |
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| DOID:2747 | glycogen storage disease | HGNC:8877 | Homo sapiens (human) | 5213 | PFKM |
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| DOID:11721 | glycogen storage disease VII | HGNC:8877 | Homo sapiens (human) | 5213 | PFKM |
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| DOID:0014667 | disease of metabolism | HGNC:8877 | Homo sapiens (human) | 5213 | PFKM |
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| DOID:0014667 | disease of metabolism | HGNC:8876 | Homo sapiens (human) | 5211 | PFKL |
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| DOID:2747 | glycogen storage disease | HGNC:8876 | Homo sapiens (human) | 5211 | PFKL |
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| DOID:2018 | hyperinsulinism | HGNC:8872 | Homo sapiens (human) | 5207 | PFKFB1 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | HGNC:33882 | Homo sapiens (human) | 51763 | INPP5K |
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