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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:5138 | leiomyomatosis | HGNC:1681 | Homo sapiens (human) | 960 | CD44 |
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| DOID:14502 | cholesterol ester storage disease | HGNC:6617 | Homo sapiens (human) | 3988 | LIPA |
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| DOID:0111182 | familial hemiplegic migraine 2 | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:12716 | newborn respiratory distress syndrome | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:7575 | pancreatic intraductal papillary-mucinous neoplasm | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:9538 | multiple myeloma | HGNC:5467 | Homo sapiens (human) | 3482 | IGF2R |
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| DOID:10283 | prostate cancer | HGNC:2649 | Homo sapiens (human) | 1595 | CYP51A1 |
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| DOID:12559 | idiopathic juvenile osteoporosis | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:1184 | nephrotic syndrome | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:2921 | glomerulonephritis | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0080557 | congenital disorder of glycosylation Ie | HGNC:3005 | Homo sapiens (human) | 8813 | DPM1 |
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| DOID:10652 | Alzheimer's disease | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:12053 | cryptococcosis | HGNC:17432 | Homo sapiens (human) | 27159 | CHIA |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:10817 | Homo sapiens (human) | 8879 | SGPL1 |
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| DOID:0050127 | sinusitis | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:14330 | Parkinson's disease | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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| DOID:9970 | obesity | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
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| DOID:3526 | cerebral infarction | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
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| DOID:0050475 | Weill-Marchesani syndrome | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0111420 | familial GPIHBP1 deficiency | HGNC:24945 | Homo sapiens (human) | 338328 | GPIHBP1 |
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| DOID:900 | hepatopulmonary syndrome | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:1312 | focal segmental glomerulosclerosis | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:10316 | pneumoconiosis | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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