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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:0050741 | alcohol dependence | HGNC:14921 | Homo sapiens (human) | 50833 | TAS2R16 |
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| DOID:12177 | common variable immunodeficiency | HGNC:6006 | Homo sapiens (human) | 50615 | IL21R |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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| DOID:9119 | acute myeloid leukemia | HGNC:7989 | Homo sapiens (human) | 4893 | NRAS |
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| DOID:12365 | malaria | HGNC:7873 | Homo sapiens (human) | 4843 | NOS2 |
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| DOID:0111530 | linear nevus sebaceous syndrome | HGNC:7989 | Homo sapiens (human) | 4893 | NRAS |
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| DOID:0060230 | basal ganglia calcification | HGNC:19918 | Homo sapiens (human) | 57462 | MYORG |
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| DOID:0110174 | Charcot-Marie-Tooth disease axonal type 2L | HGNC:30171 | Homo sapiens (human) | 26353 | HSPB8 |
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| DOID:0080315 | megalencephalic leukoencephalopathy with subcortical cysts | HGNC:13308 | Homo sapiens (human) | 51704 | GPRC5B |
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| DOID:11396 | pulmonary edema | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:0080284 | developmental and epileptic encephalopathy 57 | HGNC:18866 | Homo sapiens (human) | 343450 | KCNT2 |
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| DOID:0080074 | neural tube defect | HGNC:1550 | Homo sapiens (human) | 875 | CBS |
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| DOID:1094 | attention deficit hyperactivity disorder | HGNC:947 | Homo sapiens (human) | 10458 | BAIAP2 |
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| DOID:4511 | breast angiosarcoma | HGNC:6307 | Homo sapiens (human) | 3791 | KDR |
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| DOID:0070484 | Legius syndrome | HGNC:20249 | Homo sapiens (human) | 161742 | SPRED1 |
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| DOID:2121 | ectodermal dysplasia | HGNC:9706 | Homo sapiens (human) | 5818 | NECTIN1 |
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| DOID:13404 | uveoparotid fever | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:0080837 | growth hormone insensitivity syndrome with immune dysregulation 2 | HGNC:11367 | Homo sapiens (human) | 6777 | STAT5B |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:5973 | Homo sapiens (human) | 3596 | IL13 |
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| DOID:2477 | motor peripheral neuropathy | HGNC:3239 | Homo sapiens (human) | 1959 | EGR2 |
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| DOID:8893 | psoriasis | HGNC:6002 | Homo sapiens (human) | 50604 | IL20 |
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| DOID:5339 | cyclic hematopoiesis | HGNC:3309 | Homo sapiens (human) | 1991 | ELANE |
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| DOID:8158 | complement component 5 deficiency | HGNC:1331 | Homo sapiens (human) | 727 | C5 |
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| DOID:219 | colon cancer | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
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| DOID:10123 | pigmentation disease | HGNC:16472 | Homo sapiens (human) | 51151 | SLC45A2 |
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