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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:0090064 | familial cold autoinflammatory syndrome 3 | HGNC:9066 | Homo sapiens (human) | 5336 | PLCG2 |
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| DOID:11832 | visual epilepsy | HGNC:9067 | Homo sapiens (human) | 5337 | PLD1 |
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| DOID:3498 | pancreatic ductal adenocarcinoma | HGNC:9067 | Homo sapiens (human) | 5337 | PLD1 |
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| DOID:0080633 | developmental cardiac valvular defect | HGNC:9067 | Homo sapiens (human) | 5337 | PLD1 |
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| DOID:6000 | congestive heart failure | HGNC:9068 | Homo sapiens (human) | 5338 | PLD2 |
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| DOID:11832 | visual epilepsy | HGNC:9068 | Homo sapiens (human) | 5338 | PLD2 |
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| DOID:4450 | renal cell carcinoma | HGNC:9068 | Homo sapiens (human) | 5338 | PLD2 |
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| DOID:0080633 | developmental cardiac valvular defect | HGNC:9068 | Homo sapiens (human) | 5338 | PLD2 |
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| DOID:684 | hepatocellular carcinoma | HGNC:9083 | Homo sapiens (human) | 8985 | PLOD3 |
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| DOID:1459 | hypothyroidism | HGNC:9083 | Homo sapiens (human) | 8985 | PLOD3 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:9114 | Homo sapiens (human) | 5372 | PMM1 |
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| DOID:0080552 | congenital disorder of glycosylation Ia | HGNC:9114 | Homo sapiens (human) | 5372 | PMM1 |
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| DOID:0080552 | congenital disorder of glycosylation Ia | HGNC:9115 | Homo sapiens (human) | 5373 | PMM2 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:9115 | Homo sapiens (human) | 5373 | PMM2 |
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| DOID:5212 | congenital disorder of glycosylation | HGNC:9115 | Homo sapiens (human) | 5373 | PMM2 |
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| DOID:9970 | obesity | HGNC:9155 | Homo sapiens (human) | 5406 | PNLIP |
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| DOID:10283 | prostate cancer | HGNC:9156 | Homo sapiens (human) | 5407 | PNLIPRP1 |
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| DOID:10652 | Alzheimer's disease | HGNC:92 | Homo sapiens (human) | 37 | ACADVL |
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| DOID:0080155 | very long chain acyl-CoA dehydrogenase deficiency | HGNC:92 | Homo sapiens (human) | 37 | ACADVL |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:92 | Homo sapiens (human) | 37 | ACADVL |
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| DOID:1793 | pancreatic cancer | HGNC:920 | Homo sapiens (human) | 10317 | B3GALT5 |
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| DOID:9884 | muscular dystrophy | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:0112374 | muscular dystrophy-dystroglycanopathy | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:9296 | cleft lip | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:0050700 | cardiomyopathy | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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