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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:0060041 | autism spectrum disorder | HGNC:13875 | Homo sapiens (human) | 93986 | FOXP2 |
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| DOID:1793 | pancreatic cancer | HGNC:6145 | Homo sapiens (human) | 3680 | ITGA9 |
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| DOID:0111359 | large congenital melanocytic nevus | HGNC:7989 | Homo sapiens (human) | 4893 | NRAS |
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| DOID:0110398 | retinitis pigmentosa 51 | HGNC:20087 | Homo sapiens (human) | 123016 | TTC8 |
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| DOID:0111745 | cerebellar ataxia type 43 | HGNC:7154 | Homo sapiens (human) | 4311 | MME |
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| DOID:1926 | Gaucher's disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0112029 | non-syndromic X-linked intellectual disability 50 | HGNC:11494 | Homo sapiens (human) | 6853 | SYN1 |
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| DOID:0050127 | sinusitis | HGNC:6709 | Homo sapiens (human) | 4049 | LTA |
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| DOID:1307 | dementia | HGNC:7884 | Homo sapiens (human) | 4855 | NOTCH4 |
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| DOID:0111943 | immunodeficiency 48 | HGNC:12858 | Homo sapiens (human) | 7535 | ZAP70 |
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| DOID:2316 | brain ischemia | HGNC:9460 | Homo sapiens (human) | 8858 | PROZ |
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| DOID:0060309 | syndromic X-linked intellectual disability | HGNC:12869 | Homo sapiens (human) | 7543 | ZFX |
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| DOID:2256 | osteochondrodysplasia | HGNC:6597 | Homo sapiens (human) | 3977 | LIFR |
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| DOID:2394 | ovarian cancer | HGNC:3192 | Homo sapiens (human) | 1917 | EEF1A2 |
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| DOID:0070270 | hereditary nonpolyposis colorectal cancer type 8 | HGNC:11529 | Homo sapiens (human) | 4072 | EPCAM |
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| DOID:5577 | gastrinoma | HGNC:7059 | Homo sapiens (human) | 4255 | MGMT |
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| DOID:3328 | temporal lobe epilepsy | HGNC:637 | Homo sapiens (human) | 361 | AQP4 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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| DOID:594 | panic disorder | HGNC:21072 | Homo sapiens (human) | 79694 | MANEA |
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| DOID:399 | tuberculosis | HGNC:16711 | Homo sapiens (human) | 10333 | TLR6 |
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| DOID:0081148 | common variable immunodeficiency 5 | HGNC:7315 | Homo sapiens (human) | 931 | MS4A1 |
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| DOID:1380 | endometrial cancer | HGNC:1101 | Homo sapiens (human) | 675 | BRCA2 |
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| DOID:684 | hepatocellular carcinoma | HGNC:8805 | Homo sapiens (human) | 5157 | PDGFRL |
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| DOID:11832 | visual epilepsy | HGNC:19048 | Homo sapiens (human) | 259266 | ASPM |
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| DOID:13543 | hyperparathyroidism | HGNC:14006 | Homo sapiens (human) | 55503 | TRPV6 |
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