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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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Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References ▼ |
|---|---|---|---|---|---|---|---|---|
| DOID:898 | autosomal dominant polycystic kidney disease | WB:WBGene00004035 | Caenorhabditis elegans | 178424 | pkd-2 |
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| DOID:1227 | neutropenia | HGNC:1331 | Homo sapiens (human) | 727 | C5 |
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| DOID:4195 | hyperglycemia | RGD:62387 | Rattus norvegicus (Norway rat) | 29535 | Pdx1 |
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| DOID:10584 | retinitis pigmentosa | HGNC:2343 | Homo sapiens (human) | 23418 | CRB1 |
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| DOID:0110276 | autosomal recessive limb-girdle muscular dystrophy type 2B | MGI:1349385 | Mus musculus (house mouse) | 26903 | Dysf |
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| DOID:2513 | basal cell carcinoma | HGNC:9585 | Homo sapiens (human) | 5727 | PTCH1 |
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| DOID:0050855 | renal fibrosis | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:14330 | Parkinson's disease | HGNC:3024 | Homo sapiens (human) | 1814 | DRD3 |
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| DOID:10652 | Alzheimer's disease | FB:FBgn0284421 | Drosophila melanogaster (fruit fly) | 40260 | Psn |
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| DOID:4184 | pseudohypoparathyroidism | HGNC:4392 | Homo sapiens (human) | 2778 | GNAS |
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| DOID:0050711 | aceruloplasminemia | MGI:88476 | Mus musculus (house mouse) | 12870 | Cp |
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| DOID:0110277 | autosomal recessive limb-girdle muscular dystrophy type 2C | MGI:1346524 | Mus musculus (house mouse) | 24053 | Sgcg |
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| DOID:9074 | systemic lupus erythematosus | MGI:104879 | Mus musculus (house mouse) | 18566 | Pdcd1 |
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| DOID:14687 | diastrophic dysplasia | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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| DOID:0110280 | autosomal recessive limb-girdle muscular dystrophy type 2F | MGI:1346525 | Mus musculus (house mouse) | 24052 | Sgcd |
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| DOID:0110436 | dilated cardiomyopathy 1L | MGI:1346525 | Mus musculus (house mouse) | 24052 | Sgcd |
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| DOID:13359 | Ehlers-Danlos syndrome | HGNC:930 | Homo sapiens (human) | 11285 | B4GALT7 |
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| DOID:12134 | factor VIII deficiency | HGNC:3546 | Homo sapiens (human) | 2157 | F8 |
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| DOID:1793 | pancreatic cancer | HGNC:1570 | Homo sapiens (human) | 886 | CCKAR |
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| DOID:850 | lung disease | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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| DOID:0081267 | graft-versus-host disease | RGD:3880 | Rattus norvegicus (Norway rat) | 25385 | Faslg |
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| DOID:10763 | hypertension | HGNC:3544 | Homo sapiens (human) | 2155 | F7 |
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| DOID:14761 | Greig cephalopolysyndactyly syndrome | HGNC:4319 | Homo sapiens (human) | 2737 | GLI3 |
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| DOID:0110279 | autosomal recessive limb-girdle muscular dystrophy type 2E | MGI:1346523 | Mus musculus (house mouse) | 24051 | Sgcb |
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| DOID:0110731 | neuronal ceroid lipofuscinosis 3 | MGI:107537 | Mus musculus (house mouse) | 12752 | Cln3 |
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