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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:0080759 | Fanconi renotubular syndrome 3 | HGNC:3247 | Homo sapiens (human) | 1962 | EHHADH |
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| DOID:0070063 | autosomal dominant intellectual developmental disorder 33 | HGNC:3010 | Homo sapiens (human) | 1804 | DPP6 |
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| DOID:2218 | blood platelet disease | HGNC:6156 | Homo sapiens (human) | 3690 | ITGB3 |
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| DOID:2235 | prothrombin deficiency | HGNC:3535 | Homo sapiens (human) | 2147 | F2 |
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| DOID:0110651 | long QT syndrome 10 | HGNC:10592 | Homo sapiens (human) | 6330 | SCN4B |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:5970 | Homo sapiens (human) | 3593 | IL12B |
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| DOID:9975 | cocaine dependence | HGNC:21072 | Homo sapiens (human) | 79694 | MANEA |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:53 | Homo sapiens (human) | 1244 | ABCC2 |
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| DOID:5723 | optic atrophy | HGNC:11317 | Homo sapiens (human) | 6742 | SSBP1 |
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| DOID:13375 | temporal arteritis | HGNC:3616 | Homo sapiens (human) | 2212 | FCGR2A |
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| DOID:0111551 | neurogenic scapuloperoneal syndrome Kaeser type | HGNC:2770 | Homo sapiens (human) | 1674 | DES |
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| DOID:0111909 | autosomal dominant thrombophilia due to protein C deficiency | HGNC:9451 | Homo sapiens (human) | 5624 | PROC |
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| DOID:0070205 | familial partial lipodystrophy type 4 | HGNC:9076 | Homo sapiens (human) | 5346 | PLIN1 |
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| DOID:1826 | epilepsy | HGNC:2295 | Homo sapiens (human) | 1356 | CP |
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| DOID:4621 | holoprosencephaly | HGNC:9585 | Homo sapiens (human) | 5727 | PTCH1 |
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| DOID:2559 | opiate dependence | HGNC:15998 | Homo sapiens (human) | 89795 | NAV3 |
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| DOID:11836 | clubfoot | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:0111371 | isolated hyperchlorhidrosis | HGNC:1371 | Homo sapiens (human) | 771 | CA12 |
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| DOID:13777 | epidermodysplasia verruciformis | HGNC:6023 | Homo sapiens (human) | 3574 | IL7 |
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| DOID:9452 | steatotic liver disease | HGNC:5294 | Homo sapiens (human) | 3357 | HTR2B |
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| DOID:0080822 | aspirin-induced respiratory disease | HGNC:4952 | Homo sapiens (human) | 3126 | HLA-DRB4 |
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| DOID:418 | systemic scleroderma | HGNC:19100 | Homo sapiens (human) | 149233 | IL23R |
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| DOID:1324 | lung cancer | HGNC:7218 | Homo sapiens (human) | 4353 | MPO |
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| DOID:10652 | Alzheimer's disease | HGNC:5232 | Homo sapiens (human) | 3303 | HSPA1A |
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| DOID:980 | choroidal sclerosis | HGNC:9942 | Homo sapiens (human) | 5961 | PRPH2 |
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