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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:0050535 | exudative vitreoretinopathy | MGI:108520 | Mus musculus (house mouse) | 14366 | Fzd4 |
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| DOID:2030 | anxiety disorder | MGI:96273 | Mus musculus (house mouse) | 15550 | Htr1a |
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| DOID:0050833 | orotic aciduria | WB:WBGene00011559 | Caenorhabditis elegans | 176453 | umps-1 |
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| DOID:224 | transient cerebral ischemia | RGD:2721 | Rattus norvegicus (Norway rat) | 24401 | Got1 |
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| DOID:10652 | Alzheimer's disease | RGD:3098 | Rattus norvegicus (Norway rat) | 24590 | Mme |
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| DOID:10763 | hypertension | HGNC:1929 | Homo sapiens (human) | 1113 | CHGA |
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| DOID:4483 | rhinitis | HGNC:1318 | Homo sapiens (human) | 718 | C3 |
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| DOID:9282 | ocular hypertension | HGNC:7610 | Homo sapiens (human) | 4653 | MYOC |
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| DOID:684 | hepatocellular carcinoma | HGNC:5036 | Homo sapiens (human) | 3184 | HNRNPD |
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| DOID:4989 | pancreatitis | RGD:68949 | Rattus norvegicus (Norway rat) | 116553 | Il13 |
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| DOID:4989 | pancreatitis | HGNC:5973 | Homo sapiens (human) | 3596 | IL13 |
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| DOID:0110284 | autosomal recessive limb-girdle muscular dystrophy type 2L | HGNC:27337 | Homo sapiens (human) | 203859 | ANO5 |
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| DOID:3263 | piebaldism | MGI:96677 | Mus musculus (house mouse) | 16590 | Kit |
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| DOID:0110079 | Leber congenital amaurosis 8 | MGI:2136343 | Mus musculus (house mouse) | 170788 | Crb1 |
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| DOID:0050848 | obstructive sleep apnea | HGNC:3179 | Homo sapiens (human) | 1909 | EDNRA |
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| DOID:206 | hereditary multiple exostoses | MGI:894663 | Mus musculus (house mouse) | 14042 | Ext1 |
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| DOID:10763 | hypertension | HGNC:3402 | Homo sapiens (human) | 2053 | EPHX2 |
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| DOID:3770 | pulmonary fibrosis | HGNC:8583 | Homo sapiens (human) | 5054 | SERPINE1 |
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| DOID:10763 | hypertension | RGD:3000 | Rattus norvegicus (Norway rat) | 25608 | Lep |
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| DOID:10763 | hypertension | RGD:620596 | Rattus norvegicus (Norway rat) | 117029 | Ccr5 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:14929 | Homo sapiens (human) | 23411 | SIRT1 |
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| DOID:0060041 | autism spectrum disorder | WB:WBGene00006412 | Caenorhabditis elegans | 181484 | nlg-1 |
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| DOID:3659 | sialuria | MGI:1924105 | Mus musculus (house mouse) | 235504 | Slc17a5 |
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| DOID:5082 | liver cirrhosis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:9970 | obesity | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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