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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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MIRAGE
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:0111745 | cerebellar ataxia type 43 | HGNC:7154 | Homo sapiens (human) | 4311 | MME |
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| DOID:1485 | cystic fibrosis | HGNC:5232 | Homo sapiens (human) | 3303 | HSPA1A |
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| DOID:1324 | lung cancer | HGNC:5331 | Homo sapiens (human) | 64127 | NOD2 |
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| DOID:0060892 | late onset Parkinson's disease | HGNC:7106 | Homo sapiens (human) | 4287 | ATXN3 |
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| DOID:0112363 | spondylocostal dysostosis 5 | HGNC:11605 | Homo sapiens (human) | 6911 | TBX6 |
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| DOID:2340 | craniosynostosis | HGNC:30000 | Homo sapiens (human) | 27241 | BBS9 |
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| DOID:1825 | childhood absence epilepsy | HGNC:4087 | Homo sapiens (human) | 2566 | GABRG2 |
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| DOID:1742 | drug psychosis | HGNC:4093 | Homo sapiens (human) | 2572 | GAD2 |
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| DOID:3146 | lipid metabolism disorder | HGNC:9232 | Homo sapiens (human) | 5465 | PPARA |
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| DOID:0081102 | familial gestational hyperthyroidism | HGNC:12373 | Homo sapiens (human) | 7253 | TSHR |
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| DOID:1793 | pancreatic cancer | HGNC:7218 | Homo sapiens (human) | 4353 | MPO |
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| DOID:0110551 | autosomal dominant nonsyndromic deafness 21 | HGNC:13872 | Homo sapiens (human) | 9750 | RIPOR2 |
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| DOID:12662 | paracoccidioidomycosis | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:0112173 | combined deficiency of vitamin K-dependent clotting factors 1 | HGNC:4247 | Homo sapiens (human) | 2677 | GGCX |
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| DOID:0070296 | primary autosomal recessive microcephaly | HGNC:6637 | Homo sapiens (human) | 4001 | LMNB1 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:1541 | Homo sapiens (human) | 867 | CBL |
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| DOID:2256 | osteochondrodysplasia | HGNC:12340 | Homo sapiens (human) | 7227 | TRPS1 |
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| DOID:0112166 | autosomal dominant nonsyndromic deafness 75 | HGNC:12347 | Homo sapiens (human) | 8295 | TRRAP |
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| DOID:0081267 | graft-versus-host disease | HGNC:3619 | Homo sapiens (human) | 2214 | FCGR3A |
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| DOID:11054 | urinary bladder cancer | HGNC:6844 | Homo sapiens (human) | 6416 | MAP2K4 |
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| DOID:0080061 | autosomal recessive spinocerebellar ataxia 2 | HGNC:18667 | Homo sapiens (human) | 23203 | PMPCA |
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| DOID:0070296 | primary autosomal recessive microcephaly | HGNC:24305 | Homo sapiens (human) | 9918 | NCAPD2 |
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| DOID:0081123 | X-linked mental retardation Gustavson type | HGNC:9910 | Homo sapiens (human) | 27316 | RBMX |
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| DOID:8454 | riboflavin deficiency | HGNC:30225 | Homo sapiens (human) | 55065 | SLC52A1 |
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| DOID:4483 | rhinitis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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