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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:2842 | Jervell-Lange Nielsen syndrome | MGI:108083 | Mus musculus (house mouse) | 16535 | Kcnq1 |
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| DOID:10763 | hypertension | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:10325 | silicosis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:6000 | congestive heart failure | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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| DOID:1919 | Lesch-Nyhan syndrome | MGI:96217 | Mus musculus (house mouse) | 15452 | Hprt1 |
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| DOID:9970 | obesity | HGNC:4923 | Homo sapiens (human) | 3099 | HK2 |
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| DOID:0070255 | congenital disorder of glycosylation type IIc | HGNC:20197 | Homo sapiens (human) | 55343 | SLC35C1 |
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| DOID:9352 | type 2 diabetes mellitus | MGI:104874 | Mus musculus (house mouse) | 11652 | Akt2 |
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| DOID:0050773 | paraganglioma | HGNC:10681 | Homo sapiens (human) | 6390 | SDHB |
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| DOID:0050559 | Fukuyama congenital muscular dystrophy | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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| DOID:14504 | Niemann-Pick disease | MGI:98325 | Mus musculus (house mouse) | 20597 | Smpd1 |
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| DOID:11476 | osteoporosis | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:10587 | Krabbe disease | MGI:95636 | Mus musculus (house mouse) | 14420 | Galc |
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| DOID:13141 | uveitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:9884 | muscular dystrophy | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:6000 | congestive heart failure | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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| DOID:0050560 | Walker-Warburg syndrome | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:0060849 | osteoporosis-pseudoglioma syndrome | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:0110299 | autosomal recessive limb-girdle muscular dystrophy type 2I | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:384 | Wolff-Parkinson-White syndrome | HGNC:9386 | Homo sapiens (human) | 51422 | PRKAG2 |
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| DOID:9256 | colorectal cancer | RGD:2082 | Rattus norvegicus (Norway rat) | 25233 | Akt2 |
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| DOID:9256 | colorectal cancer | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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| DOID:10763 | hypertension | RGD:2168 | Rattus norvegicus (Norway rat) | 24212 | Atp1a2 |
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| DOID:0070253 | congenital disorder of glycosylation type IIa | MGI:2384966 | Mus musculus (house mouse) | 217664 | Mgat2 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:8976 | Homo sapiens (human) | 5291 | PIK3CB |
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