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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:3082 | interstitial lung disease | HGNC:5991 | Homo sapiens (human) | 3552 | IL1A |
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| DOID:0050475 | Weill-Marchesani syndrome | HGNC:3603 | Homo sapiens (human) | 2200 | FBN1 |
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| DOID:9970 | obesity | RGD:2796 | Rattus norvegicus (Norway rat) | 25058 | Hk1 |
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| DOID:0060485 | Mowat-Wilson syndrome | MGI:1344407 | Mus musculus (house mouse) | 24136 | Zeb2 |
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| DOID:2729 | dyskeratosis congenita | MGI:1861727 | Mus musculus (house mouse) | 245474 | Dkc1 |
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| DOID:684 | hepatocellular carcinoma | MGI:97250 | Mus musculus (house mouse) | 17869 | Myc |
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| DOID:5844 | myocardial infarction | HGNC:7939 | Homo sapiens (human) | 4878 | NPPA |
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| DOID:0110475 | autosomal recessive nonsyndromic deafness 1A | MGI:107588 | Mus musculus (house mouse) | 14623 | Gjb6 |
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| DOID:206 | hereditary multiple exostoses | HGNC:3512 | Homo sapiens (human) | 2131 | EXT1 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:1667 | Homo sapiens (human) | 952 | CD38 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:1663 | Homo sapiens (human) | 948 | CD36 |
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| DOID:5844 | myocardial infarction | HGNC:8583 | Homo sapiens (human) | 5054 | SERPINE1 |
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| DOID:5419 | schizophrenia | HGNC:17328 | Homo sapiens (human) | 84062 | DTNBP1 |
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| DOID:1838 | Menkes disease | MGI:96817 | Mus musculus (house mouse) | 16948 | Lox |
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| DOID:0060062 | familial juvenile hyperuricemic nephropathy | HGNC:12559 | Homo sapiens (human) | 7369 | UMOD |
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| DOID:10763 | hypertension | RGD:2069 | Rattus norvegicus (Norway rat) | 24179 | Agt |
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| DOID:1826 | epilepsy | FB:FBgn0285944 | Drosophila melanogaster (fruit fly) | 32619 | para |
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| DOID:9119 | acute myeloid leukemia | HGNC:2348 | Homo sapiens (human) | 1387 | CREBBP |
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| DOID:10629 | microphthalmia | MGI:106911 | Mus musculus (house mouse) | 15159 | Hccs |
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| DOID:11476 | osteoporosis | MGI:1100089 | Mus musculus (house mouse) | 21943 | Tnfsf11 |
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| DOID:0060284 | paroxysmal nocturnal hemoglobinuria | HGNC:8957 | Homo sapiens (human) | 5277 | PIGA |
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| DOID:9744 | type 1 diabetes mellitus | RGD:708418 | Rattus norvegicus (Norway rat) | 84349 | Cd40lg |
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| DOID:13359 | Ehlers-Danlos syndrome | WB:WBGene00005021 | Caenorhabditis elegans | 176382 | sqv-3 |
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| DOID:14365 | systemic primary carnitine deficiency disease | HGNC:10969 | Homo sapiens (human) | 6584 | SLC22A5 |
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| DOID:10652 | Alzheimer's disease | HGNC:1912 | Homo sapiens (human) | 1103 | CHAT |
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