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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:1338 | congenital dyserythropoietic anemia | HGNC:15480 | Homo sapiens (human) | 81624 | DIAPH3 |
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| DOID:0060690 | autosomal dominant auditory neuropathy 1 | HGNC:15480 | Homo sapiens (human) | 81624 | DIAPH3 |
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| DOID:784 | chronic kidney disease | HGNC:1548 | Homo sapiens (human) | 873 | CBR1 |
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| DOID:2841 | asthma | HGNC:15478 | Homo sapiens (human) | 80332 | ADAM33 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:15478 | Homo sapiens (human) | 80332 | ADAM33 |
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| DOID:4483 | rhinitis | HGNC:15478 | Homo sapiens (human) | 80332 | ADAM33 |
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| DOID:0060041 | autism spectrum disorder | HGNC:15474 | Homo sapiens (human) | 50944 | SHANK1 |
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| DOID:3827 | congenital diaphragmatic hernia | HGNC:15472 | Homo sapiens (human) | 8854 | ALDH1A2 |
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| DOID:11198 | DiGeorge syndrome | HGNC:15472 | Homo sapiens (human) | 8854 | ALDH1A2 |
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| DOID:9970 | obesity | HGNC:15472 | Homo sapiens (human) | 8854 | ALDH1A2 |
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| DOID:0111166 | molybdenum cofactor deficiency type C | HGNC:15465 | Homo sapiens (human) | 10243 | GPHN |
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| DOID:655 | inherited metabolic disorder | HGNC:15465 | Homo sapiens (human) | 10243 | GPHN |
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| DOID:10273 | heart conduction disease | HGNC:15460 | Homo sapiens (human) | 55799 | CACNA2D3 |
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| DOID:0110346 | osteogenesis imperfecta type 10 | HGNC:1546 | Homo sapiens (human) | 871 | SERPINH1 |
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| DOID:5082 | liver cirrhosis | HGNC:1546 | Homo sapiens (human) | 871 | SERPINH1 |
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| DOID:0111144 | preterm premature rupture of the membranes | HGNC:1546 | Homo sapiens (human) | 871 | SERPINH1 |
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| DOID:0110567 | autosomal dominant nonsyndromic deafness 41 | HGNC:15459 | Homo sapiens (human) | 22953 | P2RX2 |
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| DOID:0112283 | spondyloepiphyseal dysplasia Kondo-Fu type | HGNC:15456 | Homo sapiens (human) | 8720 | MBTPS1 |
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| DOID:0060250 | idiopathic scoliosis | HGNC:15456 | Homo sapiens (human) | 8720 | MBTPS1 |
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| DOID:0080754 | X-linked keratosis follicularis spinulosa decalvans | HGNC:15455 | Homo sapiens (human) | 51360 | MBTPS2 |
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| DOID:0112012 | X-linked mutilating palmoplantar keratoderma with periorificial keratotic plaques | HGNC:15455 | Homo sapiens (human) | 51360 | MBTPS2 |
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| DOID:0111821 | ichthyosis follicularis-alopecia-photophobia syndrome 1 | HGNC:15455 | Homo sapiens (human) | 51360 | MBTPS2 |
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| DOID:0111847 | osteogenesis imperfecta type 19 | HGNC:15455 | Homo sapiens (human) | 51360 | MBTPS2 |
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| DOID:0080690 | RASopathy | HGNC:15454 | Homo sapiens (human) | 8036 | SHOC2 |
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| DOID:3310 | atopic dermatitis | HGNC:15454 | Homo sapiens (human) | 8036 | SHOC2 |
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