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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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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol ▲ | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0070112 | Niemann-Pick disease type B | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
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| DOID:14504 | Niemann-Pick disease | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
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| DOID:0070111 | Niemann-Pick disease type A | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
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| DOID:893 | Wilson disease | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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| DOID:0110339 | osteogenesis imperfecta type 3 | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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| DOID:9675 | pulmonary emphysema | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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| DOID:12347 | osteogenesis imperfecta | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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| DOID:6432 | pulmonary hypertension | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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| DOID:0110341 | osteogenesis imperfecta type 2 | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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| DOID:9406 | hypopituitarism | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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| DOID:224 | transient cerebral ischemia | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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| DOID:12140 | Chagas disease | HGNC:11177 | Homo sapiens (human) | 6646 | SOAT1 |
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| DOID:783 | end stage renal disease | HGNC:11178 | Homo sapiens (human) | 8435 | SOAT2 |
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| DOID:684 | hepatocellular carcinoma | HGNC:11178 | Homo sapiens (human) | 8435 | SOAT2 |
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| DOID:1184 | nephrotic syndrome | HGNC:11178 | Homo sapiens (human) | 8435 | SOAT2 |
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| DOID:3393 | coronary artery disease | HGNC:11178 | Homo sapiens (human) | 8435 | SOAT2 |
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| DOID:83 | cataract | SGD:S000003920 | Saccharomyces cerevisiae S288C | 853624 | SOR1 |
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| DOID:9743 | diabetic neuropathy | SGD:S000003920 | Saccharomyces cerevisiae S288C | 853624 | SOR1 |
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| DOID:0081427 | autosomal recessive distal hereditary motor neuronopathy 8 | SGD:S000003920 | Saccharomyces cerevisiae S288C | 853624 | SOR1 |
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| DOID:0081376 | obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy | SGD:S000003920 | Saccharomyces cerevisiae S288C | 853624 | SOR1 |
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| DOID:83 | cataract | SGD:S000002405 | Saccharomyces cerevisiae S288C | 851351 | SOR2 |
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| DOID:0081427 | autosomal recessive distal hereditary motor neuronopathy 8 | SGD:S000002405 | Saccharomyces cerevisiae S288C | 851351 | SOR2 |
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| DOID:9743 | diabetic neuropathy | SGD:S000002405 | Saccharomyces cerevisiae S288C | 851351 | SOR2 |
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| DOID:0081376 | obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy | SGD:S000002405 | Saccharomyces cerevisiae S288C | 851351 | SOR2 |
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