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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:5041 | esophageal cancer | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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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:2987 | familial mediterranean fever | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:289 | endometriosis | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:9269 | maple syrup urine disease | HGNC:986 | Homo sapiens (human) | 593 | BCKDHA |
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| DOID:2018 | hyperinsulinism | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:783 | end stage renal disease | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0050770 | polycystic liver disease | HGNC:9008 | Homo sapiens (human) | 5310 | PKD1 |
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| DOID:11612 | polycystic ovary syndrome | HGNC:2594 | Homo sapiens (human) | 1588 | CYP19A1 |
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| DOID:11335 | sarcoidosis | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:11758 | iron deficiency anemia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0080855 | Parkinsonism | HGNC:4244 | Homo sapiens (human) | 2675 | GFRA2 |
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| DOID:3534 | Lafora disease | HGNC:3413 | Homo sapiens (human) | 7957 | EPM2A |
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| DOID:10652 | Alzheimer's disease | HGNC:108 | Homo sapiens (human) | 43 | ACHE |
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| DOID:1612 | breast cancer | HGNC:587 | Homo sapiens (human) | 328 | APEX1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:381 | Homo sapiens (human) | 231 | AKR1B1 |
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| DOID:4440 | seminoma | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
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| DOID:5520 | head and neck squamous cell carcinoma | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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| DOID:0111108 | maturity-onset diabetes of the young type 10 | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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| DOID:14250 | Down syndrome | HGNC:14683 | Homo sapiens (human) | 23275 | POFUT2 |
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| DOID:0060233 | cardiofaciocutaneous syndrome | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:7148 | rheumatoid arthritis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0110480 | autosomal recessive nonsyndromic deafness 22 | HGNC:16378 | Homo sapiens (human) | 146183 | OTOA |
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| DOID:13832 | patent ductus arteriosus | HGNC:11743 | Homo sapiens (human) | 7021 | TFAP2B |
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