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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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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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:6000 | congestive heart failure | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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| DOID:9884 | muscular dystrophy | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:13141 | uveitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:10587 | Krabbe disease | MGI:95636 | Mus musculus (house mouse) | 14420 | Galc |
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| DOID:11476 | osteoporosis | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:14504 | Niemann-Pick disease | MGI:98325 | Mus musculus (house mouse) | 20597 | Smpd1 |
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| DOID:0050559 | Fukuyama congenital muscular dystrophy | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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| DOID:0050773 | paraganglioma | HGNC:10681 | Homo sapiens (human) | 6390 | SDHB |
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| DOID:9352 | type 2 diabetes mellitus | MGI:104874 | Mus musculus (house mouse) | 11652 | Akt2 |
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| DOID:0070255 | congenital disorder of glycosylation type IIc | HGNC:20197 | Homo sapiens (human) | 55343 | SLC35C1 |
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| DOID:9970 | obesity | HGNC:4923 | Homo sapiens (human) | 3099 | HK2 |
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| DOID:1919 | Lesch-Nyhan syndrome | MGI:96217 | Mus musculus (house mouse) | 15452 | Hprt1 |
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| DOID:6000 | congestive heart failure | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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| DOID:10325 | silicosis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:10763 | hypertension | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:2842 | Jervell-Lange Nielsen syndrome | MGI:108083 | Mus musculus (house mouse) | 16535 | Kcnq1 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:5993 | Homo sapiens (human) | 3554 | IL1R1 |
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| DOID:12802 | mucopolysaccharidosis I | HGNC:5391 | Homo sapiens (human) | 3425 | IDUA |
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| DOID:0110671 | congenital myasthenic syndrome 6 | HGNC:1912 | Homo sapiens (human) | 1103 | CHAT |
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| DOID:783 | end stage renal disease | HGNC:6344 | Homo sapiens (human) | 9365 | KL |
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| DOID:12801 | mucopolysaccharidosis III | HGNC:7632 | Homo sapiens (human) | 4669 | NAGLU |
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| DOID:3526 | cerebral infarction | HGNC:9603 | Homo sapiens (human) | 5740 | PTGIS |
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| DOID:3068 | glioblastoma | HGNC:9604 | Homo sapiens (human) | 5742 | PTGS1 |
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| DOID:3068 | glioblastoma | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:0050453 | lissencephaly | HGNC:8574 | Homo sapiens (human) | 5048 | PAFAH1B1 |
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