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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:3910 | lung adenocarcinoma | RGD:1597139 | Rattus norvegicus (Norway rat) | 361596 | Idh2 |
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| DOID:4248 | coronary stenosis | HGNC:20580 | Homo sapiens (human) | 120227 | CYP2R1 |
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| DOID:9352 | type 2 diabetes mellitus | RGD:2082 | Rattus norvegicus (Norway rat) | 25233 | Akt2 |
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| DOID:3012 | Li-Fraumeni syndrome | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:9273 | citrullinemia | HGNC:10983 | Homo sapiens (human) | 10165 | SLC25A13 |
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| DOID:2154 | nephroblastoma | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:9256 | colorectal cancer | WB:WBGene00001630 | Caenorhabditis elegans | 176736 | gly-5 |
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| DOID:0080923 | bilateral parasagittal parieto-occipital polymicrogyria | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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| DOID:13810 | familial hypercholesterolemia | MGI:106594 | Mus musculus (house mouse) | 14933 | Gk |
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| DOID:0112315 | brain small vessel disease 3 | WB:WBGene00008426 | Caenorhabditis elegans | 3565069 | D2045.9 |
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| DOID:0112313 | brain small vessel disease | HGNC:7962 | Homo sapiens (human) | 9572 | NR1D1 |
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| DOID:14735 | hereditary angioedema | Xenbase:XB-GENE-17344583 | Xenopus laevis (African clawed frog) | 108703226 | hs3st6.S |
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| DOID:0050861 | colorectal adenocarcinoma | HGNC:1681 | Homo sapiens (human) | 960 | CD44 |
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| DOID:3744 | cervical squamous cell carcinoma | HGNC:3148 | Homo sapiens (human) | 1890 | TYMP |
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| DOID:12306 | vitiligo | RGD:3870 | Rattus norvegicus (Norway rat) | 29260 | Tlr4 |
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| DOID:0080288 | spinocerebellar ataxia 46 | HGNC:17158 | Homo sapiens (human) | 23646 | PLD3 |
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| DOID:13810 | familial hypercholesterolemia | MGI:97879 | Mus musculus (house mouse) | 19662 | Rbp4 |
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| DOID:8437 | intestinal obstruction | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:0080557 | congenital disorder of glycosylation Ie | Xenbase:XB-GENE-976623 | Xenopus tropicalis (tropical clawed frog) | 496884 | dpm1 |
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| DOID:2870 | endometrial adenocarcinoma | FB:FBgn0026597 | Drosophila melanogaster (fruit fly) | 43565 | Axn |
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| DOID:9452 | steatotic liver disease | RGD:3932 | Rattus norvegicus (Norway rat) | 54315 | Ucp2 |
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| DOID:0110292 | autosomal recessive limb-girdle muscular dystrophy type 2O | RGD:1359396 | Rattus norvegicus (Norway rat) | 362567 | Pomgnt1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:4323 | Homo sapiens (human) | 2739 | GLO1 |
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| DOID:5844 | myocardial infarction | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
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| DOID:0111063 | hyperphosphatemic familial tumoral calcinosis | HGNC:6344 | Homo sapiens (human) | 9365 | KL |
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