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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:1214 | tympanosclerosis | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
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| DOID:10754 | otitis media | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
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| DOID:13207 | proliferative diabetic retinopathy | HGNC:3357 | Homo sapiens (human) | 5168 | ENPP2 |
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| DOID:0060774 | congenital diarrhea | HGNC:16526 | Homo sapiens (human) | 51703 | ACSL5 |
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| DOID:4914 | esophagus adenocarcinoma | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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| DOID:3125 | multiple endocrine neoplasia | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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| DOID:11983 | Prader-Willi syndrome | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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| DOID:783 | end stage renal disease | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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| DOID:3525 | middle cerebral artery infarction | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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| DOID:1287 | cardiovascular system disease | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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| DOID:11981 | morbid obesity | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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| DOID:9743 | diabetic neuropathy | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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| DOID:9970 | obesity | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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| DOID:0050848 | obstructive sleep apnea | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | HGNC:33882 | Homo sapiens (human) | 51763 | INPP5K |
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| DOID:0080197 | congenital muscular dystrophy with cataracts and intellectual disability | HGNC:33882 | Homo sapiens (human) | 51763 | INPP5K |
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| DOID:2018 | hyperinsulinism | HGNC:8872 | Homo sapiens (human) | 5207 | PFKFB1 |
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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: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: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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