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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:684 | hepatocellular carcinoma | HGNC:16636 | Homo sapiens (human) | 23095 | KIF1B |
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| DOID:0050890 | synucleinopathy | HGNC:16636 | Homo sapiens (human) | 23095 | KIF1B |
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| DOID:2377 | multiple sclerosis | HGNC:16636 | Homo sapiens (human) | 23095 | KIF1B |
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| DOID:769 | neuroblastoma | HGNC:16636 | Homo sapiens (human) | 23095 | KIF1B |
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| DOID:11714 | gestational diabetes | HGNC:16638 | Homo sapiens (human) | 10250 | SRRM1 |
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| DOID:1574 | alcohol use disorder | HGNC:16639 | Homo sapiens (human) | 23524 | SRRM2 |
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| DOID:14330 | Parkinson's disease | HGNC:16639 | Homo sapiens (human) | 23524 | SRRM2 |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:16639 | Homo sapiens (human) | 23524 | SRRM2 |
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| DOID:10003 | sensorineural hearing loss | HGNC:1664 | Homo sapiens (human) | 949 | SCARB1 |
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| DOID:783 | end stage renal disease | HGNC:1664 | Homo sapiens (human) | 949 | SCARB1 |
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| DOID:418 | systemic scleroderma | HGNC:16642 | Homo sapiens (human) | 58191 | CXCL16 |
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| DOID:0080600 | COVID-19 | HGNC:16642 | Homo sapiens (human) | 58191 | CXCL16 |
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| DOID:418 | systemic scleroderma | HGNC:16647 | Homo sapiens (human) | 10663 | CXCR6 |
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| 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:0111469 | combined oxidative phosphorylation deficiency 16 | HGNC:16650 | Homo sapiens (human) | 65080 | MRPL44 |
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| DOID:5426 | primary ovarian insufficiency | HGNC:16654 | Homo sapiens (human) | 54534 | MRPL50 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:1667 | Homo sapiens (human) | 952 | CD38 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:1667 | Homo sapiens (human) | 952 | CD38 |
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| DOID:1508 | candidiasis | HGNC:16673 | Homo sapiens (human) | 81611 | ANP32E |
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| DOID:1508 | candidiasis | HGNC:16677 | Homo sapiens (human) | 10541 | ANP32B |
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| DOID:0080107 | microcephaly and chorioretinopathy 3 | HGNC:16691 | Homo sapiens (human) | 27229 | TUBGCP4 |
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| DOID:0060741 | methylmalonic acidemia due to transcobalamin receptor defect | HGNC:16692 | Homo sapiens (human) | 51293 | CD320 |
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| DOID:11446 | sciatic neuropathy | HGNC:16696 | Homo sapiens (human) | 22938 | SNW1 |
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| DOID:1793 | pancreatic cancer | HGNC:16696 | Homo sapiens (human) | 22938 | SNW1 |
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