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GlyTouCan
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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▲ | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0111948 | immunodeficiency 46 | HGNC:11763 | Homo sapiens (human) | 7037 | TFRC |
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| DOID:2394 | ovarian cancer | HGNC:3430 | Homo sapiens (human) | 2064 | ERBB2 |
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| DOID:13241 | Behcet's disease | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0060558 | lethal congenital contracture syndrome | HGNC:237 | Homo sapiens (human) | 112 | ADCY6 |
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| DOID:0050564 | autosomal dominant nonsyndromic deafness | HGNC:19070 | Homo sapiens (human) | 9984 | THOC1 |
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| DOID:2349 | arteriosclerosis | HGNC:13886 | Homo sapiens (human) | 64240 | ABCG5 |
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| DOID:0081108 | keratosis palmoplantaris striata 1 | HGNC:3048 | Homo sapiens (human) | 1828 | DSG1 |
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| DOID:0080652 | calcium oxalate nephrolithiasis | HGNC:10993 | Homo sapiens (human) | 10861 | SLC26A1 |
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| DOID:1407 | anterior uveitis | HGNC:4883 | Homo sapiens (human) | 3075 | CFH |
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| DOID:12930 | dilated cardiomyopathy | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:1100 | Homo sapiens (human) | 672 | BRCA1 |
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| DOID:13099 | Moyamoya disease | HGNC:21625 | Homo sapiens (human) | 55107 | ANO1 |
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| DOID:2154 | nephroblastoma | HGNC:5467 | Homo sapiens (human) | 3482 | IGF2R |
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| DOID:0081001 | Cowden syndrome 5 | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:4423 | sea-blue histiocytosis | HGNC:613 | Homo sapiens (human) | 348 | APOE |
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| DOID:0080561 | congenital disorder of glycosylation Ii | HGNC:23159 | Homo sapiens (human) | 85365 | ALG2 |
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| DOID:10892 | hypospadias | HGNC:5218 | Homo sapiens (human) | 3284 | HSD3B2 |
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| DOID:3910 | lung adenocarcinoma | HGNC:9673 | Homo sapiens (human) | 5795 | PTPRJ |
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| DOID:0111589 | COACH syndrome | HGNC:28396 | Homo sapiens (human) | 91147 | TMEM67 |
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| DOID:0070053 | autosomal dominant intellectual developmental disorder 23 | HGNC:25566 | Homo sapiens (human) | 55209 | SETD5 |
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| DOID:1324 | lung cancer | HGNC:1959 | Homo sapiens (human) | 1138 | CHRNA5 |
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| DOID:10211 | cholelithiasis | HGNC:2593 | Homo sapiens (human) | 1586 | CYP17A1 |
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| DOID:11678 | onchocerciasis | HGNC:4938 | Homo sapiens (human) | 3113 | HLA-DPA1 |
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| DOID:3144 | cutis laxa | HGNC:3218 | Homo sapiens (human) | 2202 | EFEMP1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:4886 | Homo sapiens (human) | 3077 | HFE |
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