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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:0080153 | medium chain acyl-CoA dehydrogenase deficiency | MGI:87867 | Mus musculus (house mouse) | 11364 | Acadm |
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| DOID:9452 | steatotic liver disease | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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| DOID:0060363 | glycerol kinase deficiency | MGI:106594 | Mus musculus (house mouse) | 14933 | Gk |
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| DOID:1391 | Norum disease | HGNC:6522 | Homo sapiens (human) | 3931 | LCAT |
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| DOID:3070 | high grade glioma | HGNC:23059 | Homo sapiens (human) | 63827 | BCAN |
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| DOID:3803 | Crigler-Najjar syndrome | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:0110958 | Gaucher's disease type II | MGI:95665 | Mus musculus (house mouse) | 14466 | Gba1 |
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| DOID:9970 | obesity | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:12801 | mucopolysaccharidosis III | HGNC:10818 | Homo sapiens (human) | 6448 | SGSH |
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| DOID:10591 | pre-eclampsia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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| DOID:0050560 | Walker-Warburg syndrome | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:9268 | glycine encephalopathy | HGNC:4313 | Homo sapiens (human) | 2731 | GLDC |
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| DOID:9975 | cocaine dependence | RGD:61800 | Rattus norvegicus (Norway rat) | 29595 | Htr2a |
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| DOID:2843 | long QT syndrome | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
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| DOID:0050559 | Fukuyama congenital muscular dystrophy | MGI:2179507 | Mus musculus (house mouse) | 246179 | Fktn |
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| DOID:0060887 | ossification of the posterior longitudinal ligament of spine | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
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| DOID:4450 | renal cell carcinoma | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:0060867 | macrocephaly-autism syndrome | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:684 | hepatocellular carcinoma | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:10588 | adrenoleukodystrophy | HGNC:29567 | Homo sapiens (human) | 23205 | ACSBG1 |
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| DOID:9970 | obesity | HGNC:5209 | Homo sapiens (human) | 3291 | HSD11B2 |
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| DOID:13088 | periventricular leukomalacia | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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| DOID:2741 | bilirubin metabolic disorder | RGD:3935 | Rattus norvegicus (Norway rat) | 24861 | Ugt1a1 |
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