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GlyTouCan
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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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:0050866 | oral squamous cell carcinoma | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
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| DOID:1793 | pancreatic cancer | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0060193 | amyotrophic lateral sclerosis type 1 | HGNC:9461 | Homo sapiens (human) | 5630 | PRPH |
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| DOID:3121 | gallbladder cancer | HGNC:1606 | Homo sapiens (human) | 1234 | CCR5 |
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| DOID:2256 | osteochondrodysplasia | HGNC:2185 | Homo sapiens (human) | 1300 | COL10A1 |
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| DOID:0112195 | spondyloperipheral dysplasia | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:11166 | Human papillomavirus infectious disease | HGNC:3690 | Homo sapiens (human) | 2261 | FGFR3 |
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| DOID:988 | mitral valve prolapse | HGNC:4932 | Homo sapiens (human) | 3106 | HLA-B |
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| DOID:2377 | multiple sclerosis | HGNC:30308 | Homo sapiens (human) | 56963 | RGMA |
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| DOID:784 | chronic kidney disease | HGNC:2300 | Homo sapiens (human) | 1361 | CPB2 |
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| DOID:9119 | acute myeloid leukemia | HGNC:6998 | Homo sapiens (human) | 4210 | MEFV |
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| DOID:2626 | choroid plexus papilloma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:10652 | Alzheimer's disease | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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| DOID:0070174 | spermatogenic failure 17 | HGNC:19218 | Homo sapiens (human) | 89869 | PLCZ1 |
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| DOID:3407 | carotid artery disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:9538 | multiple myeloma | HGNC:3616 | Homo sapiens (human) | 2212 | FCGR2A |
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| DOID:3213 | demyelinating disease | HGNC:6367 | Homo sapiens (human) | 5653 | KLK6 |
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| DOID:3146 | lipid metabolism disorder | HGNC:7530 | Homo sapiens (human) | 4598 | MVK |
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| DOID:10652 | Alzheimer's disease | HGNC:4601 | Homo sapiens (human) | 2896 | GRN |
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| DOID:768 | retinoblastoma | HGNC:7468 | Homo sapiens (human) | 4548 | MTR |
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| DOID:2247 | spondylosis | HGNC:6344 | Homo sapiens (human) | 9365 | KL |
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| DOID:0080555 | congenital disorder of glycosylation Ic | HGNC:23157 | Homo sapiens (human) | 29929 | ALG6 |
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| DOID:3393 | coronary artery disease | HGNC:8583 | Homo sapiens (human) | 5054 | SERPINE1 |
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| DOID:11716 | prediabetes syndrome | HGNC:1603 | Homo sapiens (human) | 729230 | CCR2 |
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| DOID:83 | cataract | HGNC:20893 | Homo sapiens (human) | 54880 | BCOR |
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