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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:0050811 | congenital adrenal hyperplasia | HGNC:2591 | Homo sapiens (human) | 1584 | CYP11B1 |
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| DOID:10652 | Alzheimer's disease | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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| DOID:1073 | renal hypertension | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:10763 | hypertension | HGNC:5218 | Homo sapiens (human) | 3284 | HSD3B2 |
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| DOID:0110178 | Charcot-Marie-Tooth disease axonal type 2V | HGNC:7632 | Homo sapiens (human) | 4669 | NAGLU |
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| DOID:3827 | congenital diaphragmatic hernia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0080199 | colorectal carcinoma | HGNC:6919 | Homo sapiens (human) | 8930 | MBD4 |
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| DOID:0111910 | spermatogenic failure | HGNC:8807 | Homo sapiens (human) | 5161 | PDHA2 |
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| DOID:676 | juvenile rheumatoid arthritis | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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| DOID:6000 | congestive heart failure | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:12347 | osteogenesis imperfecta | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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| DOID:2842 | Jervell-Lange Nielsen syndrome | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
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| DOID:0002116 | pterygium | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:1612 | breast cancer | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:14018 | alcoholic liver cirrhosis | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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| DOID:11162 | respiratory failure | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:13608 | biliary atresia | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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| DOID:0060189 | ileitis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:0110292 | autosomal recessive limb-girdle muscular dystrophy type 2O | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:2870 | endometrial adenocarcinoma | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:898 | autosomal dominant polycystic kidney disease | HGNC:9009 | Homo sapiens (human) | 5311 | PKD2 |
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| DOID:0090101 | lethal congenital glycogen storage disease of heart | HGNC:9386 | Homo sapiens (human) | 51422 | PRKAG2 |
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| DOID:2615 | papilloma | HGNC:9035 | Homo sapiens (human) | 5321 | PLA2G4A |
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| DOID:224 | transient cerebral ischemia | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:409 | liver disease | HGNC:9411 | Homo sapiens (human) | 5589 | PRKCSH |
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