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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:8481 | rheumatic myocarditis | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:9452 | steatotic liver disease | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:2671 | transitional cell carcinoma | HGNC:1681 | Homo sapiens (human) | 960 | CD44 |
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| DOID:1920 | hyperuricemia | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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| DOID:0111237 | congenital muscular dystrophy-dystroglycanopathy type A1 | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:1184 | nephrotic syndrome | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | HGNC:22954 | Homo sapiens (human) | 56983 | POGLUT1 |
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| DOID:11394 | adult respiratory distress syndrome | HGNC:9031 | Homo sapiens (human) | 5320 | PLA2G2A |
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| DOID:0050700 | cardiomyopathy | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:557 | kidney disease | HGNC:8638 | Homo sapiens (human) | 8850 | KAT2B |
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| DOID:10534 | stomach cancer | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:12662 | paracoccidioidomycosis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0080821 | exercise-induced bronchoconstriction | HGNC:435 | Homo sapiens (human) | 240 | ALOX5 |
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| DOID:13042 | persistent fetal circulation syndrome | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:0050933 | ovarian serous carcinoma | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
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| DOID:1184 | nephrotic syndrome | HGNC:93 | Homo sapiens (human) | 38 | ACAT1 |
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| DOID:8577 | ulcerative colitis | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:1380 | endometrial cancer | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:2841 | asthma | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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| DOID:5409 | lung small cell carcinoma | HGNC:2602 | Homo sapiens (human) | 1591 | CYP24A1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:5217 | Homo sapiens (human) | 3283 | HSD3B1 |
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| DOID:0111040 | glycogen storage disease IXd | HGNC:8925 | Homo sapiens (human) | 5255 | PHKA1 |
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| DOID:0080162 | lupus nephritis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:16825 | Homo sapiens (human) | 55613 | MTMR8 |
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| DOID:3393 | coronary artery disease | HGNC:6344 | Homo sapiens (human) | 9365 | KL |
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