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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:9452 | steatotic liver disease | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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| DOID:0060740 | methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency | HGNC:7526 | Homo sapiens (human) | 4594 | MMUT |
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| DOID:12365 | malaria | HGNC:9020 | Homo sapiens (human) | 5313 | PKLR |
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| DOID:9970 | obesity | HGNC:6554 | Homo sapiens (human) | 3953 | LEPR |
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| DOID:0110635 | muscular dystrophy-dystroglycanopathy type B5 | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:0060284 | paroxysmal nocturnal hemoglobinuria | HGNC:8957 | Homo sapiens (human) | 5277 | PIGA |
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| DOID:0110295 | autosomal recessive limb-girdle muscular dystrophy type 2U | HGNC:37276 | Homo sapiens (human) | 729920 | CRPPA |
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| DOID:0110657 | congenital myasthenic syndrome 8 | HGNC:329 | Homo sapiens (human) | 375790 | AGRN |
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| DOID:0050833 | orotic aciduria | HGNC:12563 | Homo sapiens (human) | 7372 | UMPS |
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| DOID:2747 | glycogen storage disease | HGNC:8931 | Homo sapiens (human) | 5261 | PHKG2 |
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| DOID:0070257 | congenital disorder of glycosylation type IIe | HGNC:18622 | Homo sapiens (human) | 91949 | COG7 |
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| DOID:0050441 | mucosulfatidosis | HGNC:20376 | Homo sapiens (human) | 285362 | SUMF1 |
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| DOID:10763 | hypertension | HGNC:6554 | Homo sapiens (human) | 3953 | LEPR |
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| DOID:0112050 | non-syndromic X-linked intellectual disability 63 | HGNC:3571 | Homo sapiens (human) | 2182 | ACSL4 |
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| DOID:0110352 | retinitis pigmentosa 59 | HGNC:20603 | Homo sapiens (human) | 79947 | DHDDS |
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| DOID:0110184 | Charcot-Marie-Tooth disease type 4J | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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| DOID:3649 | pyruvate decarboxylase deficiency | HGNC:2896 | Homo sapiens (human) | 1737 | DLAT |
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| DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | HGNC:25590 | Homo sapiens (human) | 55753 | OGDHL |
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| DOID:0090140 | cortisone reductase deficiency 2 | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:0111037 | glycine N-methyltransferase deficiency | HGNC:4415 | Homo sapiens (human) | 27232 | GNMT |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:2752 | glycogen storage disease II | HGNC:4065 | Homo sapiens (human) | 2548 | GAA |
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| DOID:0050433 | fatal familial insomnia | HGNC:9449 | Homo sapiens (human) | 5621 | PRNP |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:0081168 | HMG-CoA synthase 2 deficiency | HGNC:5008 | Homo sapiens (human) | 3158 | HMGCS2 |
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