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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:0112185 | thyroid dyshormonogenesis 1 | HGNC:11040 | Homo sapiens (human) | 6528 | SLC5A5 |
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| DOID:0060001 | withdrawal disorder | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:13810 | familial hypercholesterolemia | HGNC:9205 | Homo sapiens (human) | 5445 | PON2 |
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| DOID:12365 | malaria | HGNC:6338 | Homo sapiens (human) | 3811 | KIR3DL1 |
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| DOID:8893 | psoriasis | HGNC:19100 | Homo sapiens (human) | 149233 | IL23R |
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| DOID:9975 | cocaine dependence | HGNC:8846 | Homo sapiens (human) | 8864 | PER2 |
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| DOID:2841 | asthma | HGNC:18274 | Homo sapiens (human) | 57105 | CYSLTR2 |
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| DOID:14080 | glucocorticoid-remediable aldosteronism | HGNC:2591 | Homo sapiens (human) | 1584 | CYP11B1 |
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| DOID:0070066 | autosomal dominant intellectual developmental disorder 36 | HGNC:9302 | Homo sapiens (human) | 5518 | PPP2R1A |
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| DOID:0050645 | arterial tortuosity syndrome | HGNC:13444 | Homo sapiens (human) | 81031 | SLC2A10 |
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| DOID:6000 | congestive heart failure | HGNC:283 | Homo sapiens (human) | 152 | ADRA2C |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:29284 | Homo sapiens (human) | 57609 | DIP2B |
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| DOID:1588 | thrombocytopenia | HGNC:23657 | Homo sapiens (human) | 10020 | GNE |
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| DOID:0060639 | permanent neonatal diabetes mellitus | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:0080444 | developmental and epileptic encephalopathy 27 | HGNC:4586 | Homo sapiens (human) | 2904 | GRIN2B |
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| DOID:2476 | hereditary spastic paraplegia | HGNC:20499 | Homo sapiens (human) | 79944 | L2HGDH |
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| DOID:0050741 | alcohol dependence | HGNC:4076 | Homo sapiens (human) | 2555 | GABRA2 |
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| DOID:0080459 | developmental and epileptic encephalopathy 12 | HGNC:15917 | Homo sapiens (human) | 23236 | PLCB1 |
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| DOID:5844 | myocardial infarction | HGNC:3662 | Homo sapiens (human) | 2244 | FGB |
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| DOID:0112343 | hereditary spastic paraplegia 82 | HGNC:8756 | Homo sapiens (human) | 5833 | PCYT2 |
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| DOID:8483 | retinal artery occlusion | HGNC:6018 | Homo sapiens (human) | 3569 | IL6 |
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| DOID:0070434 | hyperphosphatasia with impaired intellectual development syndrome 2 | HGNC:23215 | Homo sapiens (human) | 84720 | PIGO |
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| DOID:13250 | diarrhea | HGNC:3018 | Homo sapiens (human) | 1811 | SLC26A3 |
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| DOID:14330 | Parkinson's disease | HGNC:6893 | Homo sapiens (human) | 4137 | MAPT |
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| DOID:5041 | esophageal cancer | HGNC:5994 | Homo sapiens (human) | 7850 | IL1R2 |
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