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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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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:2043 | hepatitis B | FB:FBgn0026756 | Drosophila melanogaster (fruit fly) | 35307 | Ugt37A1 |
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| DOID:0070435 | hyperphosphatasia with impaired intellectual development syndrome 3 | HGNC:17893 | Homo sapiens (human) | 27315 | PGAP2 |
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| DOID:0050579 | glycogen storage disease XV | SGD:S000001766 | Saccharomyces cerevisiae S288C | 853932 | GLG1 |
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| DOID:11832 | visual epilepsy | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:1826 | epilepsy | WB:WBGene00001686 | Caenorhabditis elegans | 174578 | gpd-4 |
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| DOID:0111240 | congenital muscular dystrophy-dystroglycanopathy type A2 | SGD:S000000021 | Saccharomyces cerevisiae S288C | 851210 | PMT2 |
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| DOID:6713 | cerebrovascular disease | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:4195 | hyperglycemia | HGNC:23302 | Homo sapiens (human) | 80201 | HKDC1 |
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| DOID:11151 | cholecystolithiasis | FB:FBgn0027074 | Drosophila melanogaster (fruit fly) | 35137 | Ugt36F1 |
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| DOID:10003 | sensorineural hearing loss | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:0080240 | non-syndromic X-linked intellectual disability 106 | ZFIN:ZDB-GENE-051128-1 | Danio rerio (zebrafish) | 652952 | ogt.2 |
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| DOID:12716 | newborn respiratory distress syndrome | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:0080382 | nephrotic syndrome type 3 | HGNC:17175 | Homo sapiens (human) | 51196 | PLCE1 |
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| DOID:1612 | breast cancer | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:9452 | steatotic liver disease | RGD:2644 | Rattus norvegicus (Norway rat) | 25634 | G6pc1 |
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| DOID:10300 | Raynaud disease | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:10273 | heart conduction disease | HGNC:25575 | Homo sapiens (human) | 55224 | ETNK2 |
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| DOID:2978 | carbohydrate metabolic disorder | HGNC:11559 | Homo sapiens (human) | 6888 | TALDO1 |
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| DOID:0070460 | hereditary spastic paraplegia 90B | HGNC:20361 | Homo sapiens (human) | 171546 | SPTSSA |
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| DOID:0070256 | congenital disorder of glycosylation type IId | Xenbase:XB-GENE-17335264 | Xenopus laevis (African clawed frog) | 108712215 | b4galt1.1.L |
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| DOID:5082 | liver cirrhosis | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:9884 | muscular dystrophy | ZFIN:ZDB-GENE-070112-991 | Danio rerio (zebrafish) | 571876 | pomgnt1 |
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| DOID:90 | degenerative disc disease | FB:FBgn0003371 | Drosophila melanogaster (fruit fly) | 31248 | sgg |
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| DOID:1793 | pancreatic cancer | ZFIN:ZDB-GENE-040426-1505 | Danio rerio (zebrafish) | 393526 | mtap |
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| DOID:11984 | hypertrophic cardiomyopathy | HGNC:10683 | Homo sapiens (human) | 6392 | SDHD |
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