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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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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:3385 | bacterial vaginosis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:4195 | hyperglycemia | HGNC:9449 | Homo sapiens (human) | 5621 | PRNP |
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| DOID:0050581 | brachydactyly | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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| DOID:10763 | hypertension | HGNC:5217 | Homo sapiens (human) | 3283 | HSD3B1 |
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| DOID:9538 | multiple myeloma | HGNC:2621 | Homo sapiens (human) | 1557 | CYP2C19 |
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| DOID:12177 | common variable immunodeficiency | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:1059 | intellectual disability | HGNC:5996 | Homo sapiens (human) | 11141 | IL1RAPL1 |
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| DOID:3068 | glioblastoma | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:162 | cancer | HGNC:8998 | Homo sapiens (human) | 8396 | PIP4K2B |
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| DOID:9452 | steatotic liver disease | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:13359 | Ehlers-Danlos syndrome | HGNC:930 | Homo sapiens (human) | 11285 | B4GALT7 |
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| DOID:0112349 | hereditary spastic paraplegia 81 | HGNC:29361 | Homo sapiens (human) | 85465 | SELENOI |
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| DOID:11198 | DiGeorge syndrome | HGNC:10979 | Homo sapiens (human) | 6576 | SLC25A1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:9603 | Homo sapiens (human) | 5740 | PTGIS |
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| DOID:219 | colon cancer | HGNC:11906 | Homo sapiens (human) | 8794 | TNFRSF10C |
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| DOID:0080459 | developmental and epileptic encephalopathy 12 | HGNC:15917 | Homo sapiens (human) | 23236 | PLCB1 |
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| DOID:5419 | schizophrenia | HGNC:4093 | Homo sapiens (human) | 2572 | GAD2 |
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| DOID:0050452 | mevalonic aciduria | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:8677 | perinatal necrotizing enterocolitis | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:4201 | Homo sapiens (human) | 2648 | KAT2A |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:7451 | Homo sapiens (human) | 8897 | MTMR3 |
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| DOID:3717 | gastric adenocarcinoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:5383 | Homo sapiens (human) | 3418 | IDH2 |
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| DOID:7998 | hyperthyroidism | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:0110474 | autosomal recessive nonsyndromic deafness 18B | HGNC:8516 | Homo sapiens (human) | 340990 | OTOG |
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