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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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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:8719 | in situ carcinoma | HGNC:5467 | Homo sapiens (human) | 3482 | IGF2R |
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| DOID:0060536 | mitochondrial complex I deficiency | HGNC:7707 | Homo sapiens (human) | 4719 | NDUFS1 |
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| DOID:2018 | hyperinsulinism | HGNC:6709 | Homo sapiens (human) | 4049 | LTA |
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| DOID:5520 | head and neck squamous cell carcinoma | HGNC:11904 | Homo sapiens (human) | 8797 | TNFRSF10A |
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| DOID:0110092 | short-rib thoracic dysplasia 6 with or without polydactyly | HGNC:7744 | Homo sapiens (human) | 4750 | NEK1 |
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| DOID:0050861 | colorectal adenocarcinoma | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:0080730 | Ehlers-Danlos syndrome cardiac valvular type | HGNC:2198 | Homo sapiens (human) | 1278 | COL1A2 |
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| DOID:13025 | retinopathy of prematurity | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:0060874 | isolated growth hormone deficiency type IB | HGNC:4266 | Homo sapiens (human) | 2692 | GHRHR |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:381 | Homo sapiens (human) | 231 | AKR1B1 |
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| DOID:0060822 | syndromic X-linked intellectual disability Cabezas type | HGNC:2555 | Homo sapiens (human) | 8450 | CUL4B |
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| DOID:5844 | myocardial infarction | HGNC:1603 | Homo sapiens (human) | 729230 | CCR2 |
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| DOID:0080317 | megalencephalic leukoencephalopathy with subcortical cysts 2B | HGNC:26361 | Homo sapiens (human) | 220296 | HEPACAM |
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| DOID:7693 | abdominal aortic aneurysm | HGNC:7432 | Homo sapiens (human) | 4522 | MTHFD1 |
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| DOID:0081128 | mandibuloacral dysplasia type A lipodystrophy | HGNC:6636 | Homo sapiens (human) | 4000 | LMNA |
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| DOID:8778 | Crohn's disease | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:12449 | aplastic anemia | HGNC:2890 | Homo sapiens (human) | 1736 | DKC1 |
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| DOID:0050792 | multiple cutaneous and mucosal venous malformations | HGNC:11724 | Homo sapiens (human) | 7010 | TEK |
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| DOID:2942 | bronchiolitis | HGNC:7516 | Homo sapiens (human) | 727897 | MUC5B |
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| DOID:2377 | multiple sclerosis | HGNC:7158 | Homo sapiens (human) | 4321 | MMP12 |
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| DOID:1205 | allergic disease | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:2349 | arteriosclerosis | HGNC:435 | Homo sapiens (human) | 240 | ALOX5 |
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| DOID:2218 | blood platelet disease | HGNC:14388 | Homo sapiens (human) | 51206 | GP6 |
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| DOID:0090131 | complex cortical dysplasia with other brain malformations | HGNC:24036 | Homo sapiens (human) | 10297 | APC2 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:13726 | Homo sapiens (human) | 58508 | KMT2C |
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