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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:0112380 | muscular dystrophy-dystroglycanopathy type B2 | SGD:S000000021 | Saccharomyces cerevisiae S288C | 851210 | PMT2 |
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| DOID:0110298 | autosomal recessive limb-girdle muscular dystrophy type 2N | SGD:S000000021 | Saccharomyces cerevisiae S288C | 851210 | PMT2 |
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| DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | SGD:S000000021 | Saccharomyces cerevisiae S288C | 851210 | PMT2 |
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| DOID:0050560 | Walker-Warburg syndrome | SGD:S000000021 | Saccharomyces cerevisiae S288C | 851210 | PMT2 |
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| DOID:0111240 | congenital muscular dystrophy-dystroglycanopathy type A2 | SGD:S000000021 | Saccharomyces cerevisiae S288C | 851210 | PMT2 |
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| DOID:0112374 | muscular dystrophy-dystroglycanopathy | SGD:S000000021 | Saccharomyces cerevisiae S288C | 851210 | PMT2 |
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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: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:0050570 | congenital disorder of glycosylation type I | SGD:S000000805 | Saccharomyces cerevisiae S288C | 856720 | PMI40 |
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| DOID:0080554 | congenital disorder of glycosylation Ib | SGD:S000000805 | Saccharomyces cerevisiae S288C | 856720 | PMI40 |
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| DOID:2978 | carbohydrate metabolic disorder | SGD:S000000805 | Saccharomyces cerevisiae S288C | 856720 | PMI40 |
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| DOID:1612 | breast cancer | HGNC:23531 | Homo sapiens (human) | 196051 | PLPP4 |
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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:9074 | systemic lupus erythematosus | HGNC:23792 | Homo sapiens (human) | 122618 | PLD4 |
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| DOID:0080288 | spinocerebellar ataxia 46 | HGNC:17158 | Homo sapiens (human) | 23646 | PLD3 |
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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: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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