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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:2843 | long QT syndrome | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
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| DOID:9975 | cocaine dependence | RGD:61800 | Rattus norvegicus (Norway rat) | 29595 | Htr2a |
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| DOID:9268 | glycine encephalopathy | HGNC:4313 | Homo sapiens (human) | 2731 | GLDC |
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| DOID:0050560 | Walker-Warburg syndrome | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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| DOID:10591 | pre-eclampsia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:12801 | mucopolysaccharidosis III | HGNC:10818 | Homo sapiens (human) | 6448 | SGSH |
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| DOID:9970 | obesity | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:0110958 | Gaucher's disease type II | MGI:95665 | Mus musculus (house mouse) | 14466 | Gba1 |
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| DOID:3803 | Crigler-Najjar syndrome | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:3070 | high grade glioma | HGNC:23059 | Homo sapiens (human) | 63827 | BCAN |
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| DOID:1391 | Norum disease | HGNC:6522 | Homo sapiens (human) | 3931 | LCAT |
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| DOID:0060363 | glycerol kinase deficiency | MGI:106594 | Mus musculus (house mouse) | 14933 | Gk |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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| DOID:9452 | steatotic liver disease | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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| DOID:0080153 | medium chain acyl-CoA dehydrogenase deficiency | MGI:87867 | Mus musculus (house mouse) | 11364 | Acadm |
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| DOID:10763 | hypertension | HGNC:2642 | Homo sapiens (human) | 1579 | CYP4A11 |
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| DOID:1612 | breast cancer | MGI:98834 | Mus musculus (house mouse) | 22059 | Trp53 |
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| DOID:0090129 | carnitine palmitoyltransferase I deficiency | MGI:1098296 | Mus musculus (house mouse) | 12894 | Cpt1a |
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| DOID:10763 | hypertension | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:206 | hereditary multiple exostoses | MGI:108050 | Mus musculus (house mouse) | 14043 | Ext2 |
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| DOID:8677 | perinatal necrotizing enterocolitis | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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| DOID:9352 | type 2 diabetes mellitus | MGI:104663 | Mus musculus (house mouse) | 16846 | Lep |
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| DOID:3012 | Li-Fraumeni syndrome | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:684 | hepatocellular carcinoma | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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