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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:10591 | pre-eclampsia | HGNC:2606 | Homo sapiens (human) | 1594 | CYP27B1 |
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| DOID:520 | aortic disease | HGNC:12663 | Homo sapiens (human) | 7412 | VCAM1 |
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| DOID:0080351 | CLOVES syndrome | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:9976 | heroin dependence | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:8398 | osteoarthritis | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:0050144 | Kartagener syndrome | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:9970 | obesity | HGNC:5213 | Homo sapiens (human) | 3295 | HSD17B4 |
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| DOID:8778 | Crohn's disease | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:13809 | familial combined hyperlipidemia | HGNC:438 | Homo sapiens (human) | 249 | ALPL |
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| DOID:7148 | rheumatoid arthritis | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:1380 | endometrial cancer | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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| DOID:648 | kuru | HGNC:9449 | Homo sapiens (human) | 5621 | PRNP |
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| DOID:0110296 | autosomal recessive limb-girdle muscular dystrophy type 2M | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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| DOID:0080322 | polycystic kidney disease | HGNC:9035 | Homo sapiens (human) | 5321 | PLA2G4A |
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| DOID:2987 | familial mediterranean fever | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:2978 | carbohydrate metabolic disorder | HGNC:7216 | Homo sapiens (human) | 4351 | MPI |
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| DOID:6432 | pulmonary hypertension | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:0060060 | non-Hodgkin lymphoma | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:0050699 | Dent disease | HGNC:8108 | Homo sapiens (human) | 4952 | OCRL |
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| DOID:5082 | liver cirrhosis | HGNC:9053 | Homo sapiens (human) | 5329 | PLAUR |
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| DOID:11612 | polycystic ovary syndrome | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:684 | hepatocellular carcinoma | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:2748 | glycogen storage disease III | HGNC:321 | Homo sapiens (human) | 178 | AGL |
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| DOID:10283 | prostate cancer | HGNC:2665 | Homo sapiens (human) | 1604 | CD55 |
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| DOID:0112275 | developmental and epileptic encephalopathy 93 | HGNC:851 | Homo sapiens (human) | 523 | ATP6V1A |
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