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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:13099 | Moyamoya disease | HGNC:130 | Homo sapiens (human) | 59 | ACTA2 |
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| DOID:0070048 | GAND syndrome | HGNC:30778 | Homo sapiens (human) | 57459 | GATAD2B |
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| DOID:13374 | fibrodysplasia ossificans progressiva | HGNC:171 | Homo sapiens (human) | 90 | ACVR1 |
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| DOID:0110011 | advanced sleep phase syndrome 1 | HGNC:8846 | Homo sapiens (human) | 8864 | PER2 |
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| DOID:0060810 | syndromic X-linked intellectual disability type 10 | HGNC:4800 | Homo sapiens (human) | 3028 | HSD17B10 |
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| DOID:0110629 | Wolfram syndrome 1 | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:0110943 | autosomal recessive osteopetrosis 2 | HGNC:11926 | Homo sapiens (human) | 8600 | TNFSF11 |
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| DOID:12800 | mucopolysaccharidosis VI | HGNC:714 | Homo sapiens (human) | 411 | ARSB |
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| DOID:0110841 | Usher syndrome type 3A | HGNC:12605 | Homo sapiens (human) | 7401 | CLRN1 |
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| DOID:0050884 | triosephosphate isomerase deficiency | HGNC:12009 | Homo sapiens (human) | 7167 | TPI1 |
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| DOID:0070044 | Coffin-Siris syndrome 2 | HGNC:11110 | Homo sapiens (human) | 8289 | ARID1A |
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| DOID:0060688 | arteriovenous malformations of the brain | HGNC:6407 | Homo sapiens (human) | 3845 | KRAS |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:11009 | Homo sapiens (human) | 6517 | SLC2A4 |
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| DOID:684 | hepatocellular carcinoma | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:10763 | hypertension | HGNC:12299 | Homo sapiens (human) | 7201 | TRHR |
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| DOID:1574 | alcohol use disorder | HGNC:8154 | Homo sapiens (human) | 4986 | OPRK1 |
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| DOID:0111182 | familial hemiplegic migraine 2 | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:0060736 | epidermolysis bullosa simplex Ogna type | HGNC:9069 | Homo sapiens (human) | 5339 | PLEC |
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| DOID:6688 | autoimmune lymphoproliferative syndrome | HGNC:11936 | Homo sapiens (human) | 356 | FASLG |
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| DOID:0112248 | 17-beta hydroxysteroid dehydrogenase 3 deficiency | HGNC:5212 | Homo sapiens (human) | 3293 | HSD17B3 |
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| DOID:0110731 | neuronal ceroid lipofuscinosis 3 | HGNC:2074 | Homo sapiens (human) | 1201 | CLN3 |
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| DOID:3070 | high grade glioma | HGNC:5382 | Homo sapiens (human) | 3417 | IDH1 |
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| DOID:0050436 | mulibrey nanism | HGNC:7523 | Homo sapiens (human) | 4591 | TRIM37 |
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| DOID:14330 | Parkinson's disease | HGNC:11741 | Homo sapiens (human) | 7019 | TFAM |
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