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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:891 | progressive myoclonus epilepsy | HGNC:1665 | Homo sapiens (human) | 950 | SCARB2 |
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| DOID:0111444 | progressive myoclonus epilepsy 4 | HGNC:1665 | Homo sapiens (human) | 950 | SCARB2 |
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| DOID:90 | degenerative disc disease | HGNC:220 | Homo sapiens (human) | 9507 | ADAMTS4 |
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| DOID:224 | transient cerebral ischemia | HGNC:220 | Homo sapiens (human) | 9507 | ADAMTS4 |
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| DOID:7148 | rheumatoid arthritis | HGNC:220 | Homo sapiens (human) | 9507 | ADAMTS4 |
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| DOID:9970 | obesity | HGNC:220 | Homo sapiens (human) | 9507 | ADAMTS4 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:220 | Homo sapiens (human) | 9507 | ADAMTS4 |
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| DOID:0060366 | Hennekam syndrome | HGNC:219 | Homo sapiens (human) | 9508 | ADAMTS3 |
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| DOID:13359 | Ehlers-Danlos syndrome | HGNC:218 | Homo sapiens (human) | 9509 | ADAMTS2 |
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| DOID:0080733 | Ehlers-Danlos syndrome dermatosparaxis type | HGNC:218 | Homo sapiens (human) | 9509 | ADAMTS2 |
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| DOID:5844 | myocardial infarction | HGNC:217 | Homo sapiens (human) | 9510 | ADAMTS1 |
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| DOID:224 | transient cerebral ischemia | HGNC:217 | Homo sapiens (human) | 9510 | ADAMTS1 |
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| DOID:5199 | ureteral obstruction | HGNC:217 | Homo sapiens (human) | 9510 | ADAMTS1 |
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| DOID:5200 | urinary tract obstruction | HGNC:217 | Homo sapiens (human) | 9510 | ADAMTS1 |
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| DOID:11832 | visual epilepsy | HGNC:217 | Homo sapiens (human) | 9510 | ADAMTS1 |
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| DOID:2316 | brain ischemia | HGNC:217 | Homo sapiens (human) | 9510 | ADAMTS1 |
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| DOID:0060892 | late onset Parkinson's disease | HGNC:9119 | Homo sapiens (human) | 9512 | PMPCB |
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| DOID:0070332 | multiple mitochondrial dysfunctions syndrome 6 | HGNC:9119 | Homo sapiens (human) | 9512 | PMPCB |
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| DOID:14261 | fragile X syndrome | HGNC:4024 | Homo sapiens (human) | 9513 | FXR2 |
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| DOID:7474 | malignant pleural mesothelioma | HGNC:4024 | Homo sapiens (human) | 9513 | FXR2 |
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| DOID:0060041 | autism spectrum disorder | HGNC:4024 | Homo sapiens (human) | 9513 | FXR2 |
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| DOID:0110151 | Charcot-Marie-Tooth disease type 1C | HGNC:16841 | Homo sapiens (human) | 9516 | LITAF |
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| DOID:0070162 | hereditary sensory and autonomic neuropathy type 1 | HGNC:11278 | Homo sapiens (human) | 9517 | SPTLC2 |
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| DOID:0070157 | hereditary sensory and autonomic neuropathy type 1C | HGNC:11278 | Homo sapiens (human) | 9517 | SPTLC2 |
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| DOID:8893 | psoriasis | HGNC:11278 | Homo sapiens (human) | 9517 | SPTLC2 |
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