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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:11054 | urinary bladder cancer | HGNC:1511 | Homo sapiens (human) | 842 | CASP9 |
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| DOID:8893 | psoriasis | HGNC:11919 | Homo sapiens (human) | 958 | CD40 |
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| DOID:9111 | cutaneous leishmaniasis | HGNC:10907 | Homo sapiens (human) | 6556 | SLC11A1 |
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| DOID:1240 | leukemia | HGNC:79 | Homo sapiens (human) | 28 | ABO |
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| DOID:0111358 | Floating-Harbor syndrome | HGNC:16974 | Homo sapiens (human) | 10847 | SRCAP |
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| DOID:0081325 | developmental and epileptic encephalopathy 94 | HGNC:1917 | Homo sapiens (human) | 1106 | CHD2 |
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| DOID:0070274 | hereditary nonpolyposis colorectal cancer type 2 | HGNC:7127 | Homo sapiens (human) | 4292 | MLH1 |
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| DOID:5409 | lung small cell carcinoma | HGNC:3942 | Homo sapiens (human) | 2475 | MTOR |
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| DOID:0110920 | hereditary spherocytosis type 5 | HGNC:3381 | Homo sapiens (human) | 2038 | EPB42 |
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| DOID:525 | central nervous system vasculitis | HGNC:4931 | Homo sapiens (human) | 3105 | HLA-A |
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| DOID:684 | hepatocellular carcinoma | HGNC:17098 | Homo sapiens (human) | 23405 | DICER1 |
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| DOID:5844 | myocardial infarction | HGNC:2202 | Homo sapiens (human) | 1282 | COL4A1 |
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| DOID:0050156 | idiopathic pulmonary fibrosis | HGNC:18420 | Homo sapiens (human) | 29072 | SETD2 |
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| DOID:4606 | bile duct cancer | HGNC:613 | Homo sapiens (human) | 348 | APOE |
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| DOID:0070302 | multiple epiphyseal dysplasia 7 | HGNC:19721 | Homo sapiens (human) | 124583 | CANT1 |
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| DOID:0110965 | brachydactyly type A2 | HGNC:1077 | Homo sapiens (human) | 658 | BMPR1B |
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| DOID:0050848 | obstructive sleep apnea | HGNC:285 | Homo sapiens (human) | 153 | ADRB1 |
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| DOID:14184 | polyneuropathy due to drug | HGNC:3438 | Homo sapiens (human) | 2074 | ERCC6 |
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| DOID:0070511 | polyhydramnios, megalencephaly, and symptomatic epilepsy | HGNC:30172 | Homo sapiens (human) | 92335 | STRADA |
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| DOID:0110338 | osteogenesis imperfecta type 17 | HGNC:11219 | Homo sapiens (human) | 6678 | SPARC |
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| DOID:0111227 | frontotemporal dementia and/or amyotrophic lateral sclerosis 7 | HGNC:24537 | Homo sapiens (human) | 25978 | CHMP2B |
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| DOID:2394 | ovarian cancer | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:612 | primary immunodeficiency disease | HGNC:11408 | Homo sapiens (human) | 6789 | STK4 |
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| DOID:9351 | diabetes mellitus | HGNC:9668 | Homo sapiens (human) | 5789 | PTPRD |
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| DOID:986 | alopecia areata | HGNC:7884 | Homo sapiens (human) | 4855 | NOTCH4 |
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