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GlyTouCan
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:0050560 | Walker-Warburg syndrome | WB:WBGene00020924 | Caenorhabditis elegans | 189104 | W02B3.4 |
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| DOID:0050559 | Fukuyama congenital muscular dystrophy | WB:WBGene00020924 | Caenorhabditis elegans | 189104 | W02B3.4 |
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| DOID:0110296 | autosomal recessive limb-girdle muscular dystrophy type 2M | WB:WBGene00020924 | Caenorhabditis elegans | 189104 | W02B3.4 |
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| DOID:0110443 | dilated cardiomyopathy 1B | WB:WBGene00020924 | Caenorhabditis elegans | 189104 | W02B3.4 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | WB:WBGene00020924 | Caenorhabditis elegans | 189104 | W02B3.4 |
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| DOID:0080119 | mitochondrial DNA depletion syndrome 1 | HGNC:3148 | Homo sapiens (human) | 1890 | TYMP |
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| DOID:4440 | seminoma | HGNC:3148 | Homo sapiens (human) | 1890 | TYMP |
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| DOID:4948 | gallbladder carcinoma | HGNC:3148 | Homo sapiens (human) | 1890 | TYMP |
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| DOID:3307 | teratoma | HGNC:3148 | Homo sapiens (human) | 1890 | TYMP |
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| DOID:3587 | pancreatic ductal carcinoma | HGNC:3148 | Homo sapiens (human) | 1890 | TYMP |
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| DOID:0060074 | ductal carcinoma in situ | HGNC:3148 | Homo sapiens (human) | 1890 | TYMP |
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| DOID:1793 | pancreatic cancer | HGNC:3148 | Homo sapiens (human) | 1890 | TYMP |
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| DOID:3744 | cervical squamous cell carcinoma | HGNC:3148 | Homo sapiens (human) | 1890 | TYMP |
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| DOID:1380 | endometrial cancer | HGNC:3148 | Homo sapiens (human) | 1890 | TYMP |
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| DOID:2671 | transitional cell carcinoma | HGNC:3148 | Homo sapiens (human) | 1890 | TYMP |
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| DOID:4608 | common bile duct neoplasm | HGNC:3148 | Homo sapiens (human) | 1890 | TYMP |
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| DOID:11054 | urinary bladder cancer | HGNC:3148 | Homo sapiens (human) | 1890 | TYMP |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:3148 | Homo sapiens (human) | 1890 | TYMP |
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| DOID:2394 | ovarian cancer | HGNC:3148 | Homo sapiens (human) | 1890 | TYMP |
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| DOID:4450 | renal cell carcinoma | HGNC:3148 | Homo sapiens (human) | 1890 | TYMP |
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| DOID:890 | mitochondrial encephalomyopathy | HGNC:3148 | Homo sapiens (human) | 1890 | TYMP |
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| DOID:0111670 | primary hyperoxaluria type 1 | HGNC:341 | Homo sapiens (human) | 189 | AGXT |
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| DOID:2977 | primary hyperoxaluria | HGNC:341 | Homo sapiens (human) | 189 | AGXT |
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| DOID:0110296 | autosomal recessive limb-girdle muscular dystrophy type 2M | WB:WBGene00011554 | Caenorhabditis elegans | 188207 | T07A5.1 |
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| DOID:0110284 | autosomal recessive limb-girdle muscular dystrophy type 2L | WB:WBGene00011554 | Caenorhabditis elegans | 188207 | T07A5.1 |
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