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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:5844 | myocardial infarction | HGNC:7939 | Homo sapiens (human) | 4878 | NPPA |
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| DOID:0110337 | osteogenesis imperfecta type 7 | HGNC:2379 | Homo sapiens (human) | 10491 | CRTAP |
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| DOID:0050545 | visceral heterotaxy | HGNC:14357 | Homo sapiens (human) | 118856 | MMP21 |
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| DOID:0070416 | Luo-Schoch-Yamamoto syndrome | HGNC:10061 | Homo sapiens (human) | 6045 | RNF2 |
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| DOID:0080212 | polycystic kidney disease 4 | HGNC:9016 | Homo sapiens (human) | 5314 | PKHD1 |
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| DOID:10487 | Hirschsprung's disease | HGNC:3180 | Homo sapiens (human) | 1910 | EDNRB |
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| DOID:5844 | myocardial infarction | HGNC:8583 | Homo sapiens (human) | 5054 | SERPINE1 |
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| DOID:0080463 | developmental and epileptic encephalopathy 33 | HGNC:3192 | Homo sapiens (human) | 1917 | EEF1A2 |
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| DOID:14743 | trichorhinophalangeal syndrome type I | HGNC:12340 | Homo sapiens (human) | 7227 | TRPS1 |
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| DOID:0110928 | nemaline myopathy 2 | HGNC:7720 | Homo sapiens (human) | 4703 | NEB |
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| DOID:0110350 | osteogenesis imperfecta type 6 | HGNC:8824 | Homo sapiens (human) | 5176 | SERPINF1 |
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| DOID:0111442 | optic atrophy 9 | HGNC:118 | Homo sapiens (human) | 50 | ACO2 |
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| DOID:0050741 | alcohol dependence | HGNC:281 | Homo sapiens (human) | 150 | ADRA2A |
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| DOID:13482 | Proteus syndrome | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
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| DOID:10763 | hypertension | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:0050649 | atransferrinemia | HGNC:11740 | Homo sapiens (human) | 7018 | TF |
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| DOID:9970 | obesity | HGNC:6932 | Homo sapiens (human) | 4160 | MC4R |
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| DOID:12930 | dilated cardiomyopathy | HGNC:20039 | Homo sapiens (human) | 10486 | CAP2 |
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| DOID:0060700 | familial hypocalciuric hypercalcemia 1 | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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| DOID:0110615 | primary ciliary dyskinesia 25 | HGNC:21493 | Homo sapiens (human) | 161582 | DNAAF4 |
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| DOID:0081266 | pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures | HGNC:18599 | Homo sapiens (human) | 10844 | TUBGCP2 |
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| DOID:11830 | myopia | HGNC:6701 | Homo sapiens (human) | 4043 | LRPAP1 |
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| DOID:0060801 | MEHMO syndrome | HGNC:3267 | Homo sapiens (human) | 1968 | EIF2S3 |
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| DOID:0060248 | Simpson-Golabi-Behmel syndrome type 1 | HGNC:4451 | Homo sapiens (human) | 2719 | GPC3 |
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