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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
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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:5204 | fructose-1,6-bisphosphatase deficiency | SGD:S000004369 | Saccharomyces cerevisiae S288C | 851092 | FBP1 |
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| DOID:5204 | fructose-1,6-bisphosphatase deficiency | HGNC:3606 | Homo sapiens (human) | 2203 | FBP1 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:3594 | Homo sapiens (human) | 2194 | FASN |
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| DOID:9256 | colorectal cancer | HGNC:3594 | Homo sapiens (human) | 2194 | FASN |
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| DOID:0080000 | muscular disease | HGNC:3594 | Homo sapiens (human) | 2194 | FASN |
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| DOID:987 | alopecia | HGNC:25531 | Homo sapiens (human) | 55711 | FAR2 |
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| DOID:10140 | dry eye syndrome | HGNC:25531 | Homo sapiens (human) | 55711 | FAR2 |
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| DOID:0081243 | rhizomelic chondrodysplasia punctate type 4 | HGNC:26222 | Homo sapiens (human) | 84188 | FAR1 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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| DOID:6000 | congestive heart failure | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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| DOID:1574 | alcohol use disorder | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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| DOID:3146 | lipid metabolism disorder | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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| DOID:5804 | discrete subaortic stenosis | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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| DOID:9970 | obesity | HGNC:3574 | Homo sapiens (human) | 3992 | FADS1 |
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| DOID:1574 | alcohol use disorder | HGNC:3574 | Homo sapiens (human) | 3992 | FADS1 |
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| DOID:6000 | congestive heart failure | HGNC:3574 | Homo sapiens (human) | 3992 | FADS1 |
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| DOID:10763 | hypertension | HGNC:3574 | Homo sapiens (human) | 3992 | FADS1 |
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| DOID:10283 | prostate cancer | HGNC:3560 | Homo sapiens (human) | 2171 | FABP5 |
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| DOID:8893 | psoriasis | HGNC:3560 | Homo sapiens (human) | 2171 | FABP5 |
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| DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00009925 | Caenorhabditis elegans | 178364 | F52B11.2 |
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| DOID:5212 | congenital disorder of glycosylation | WB:WBGene00009925 | Caenorhabditis elegans | 178364 | F52B11.2 |
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| DOID:0080552 | congenital disorder of glycosylation Ia | WB:WBGene00009925 | Caenorhabditis elegans | 178364 | F52B11.2 |
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| DOID:0050565 | autosomal recessive nonsyndromic deafness | WB:WBGene00018175 | Caenorhabditis elegans | 185454 | F38B6.6 |
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| DOID:206 | hereditary multiple exostoses | MGI:1860765 | Mus musculus (house mouse) | 54616 | Extl3 |
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