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GlyTouCan
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:0050535 | exudative vitreoretinopathy | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:0050563 | nonsyndromic deafness | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:4079 | heart valve disease | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:0060849 | osteoporosis-pseudoglioma syndrome | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:898 | autosomal dominant polycystic kidney disease | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:0080037 | Worth syndrome | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:11476 | osteoporosis | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:10159 | osteonecrosis | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:0080567 | congenital disorder of glycosylation Ip | FB:FBgn0037108 | Drosophila melanogaster (fruit fly) | 40402 | Alg11 | CG11306 |
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| DOID:0110170 | Charcot-Marie-Tooth disease axonal type 2Q | Xenbase:XB-GENE-980614 | Xenopus laevis (African clawed frog) | 403360 | dhtkd1.L |
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| DOID:0111453 | 2-aminoadipic 2-oxoadipic aciduria | Xenbase:XB-GENE-980614 | Xenopus laevis (African clawed frog) | 403360 | dhtkd1.L |
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| DOID:332 | amyotrophic lateral sclerosis | ZFIN:ZDB-GENE-040219-1 | Danio rerio (zebrafish) | 403143 | sarm1 |
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| DOID:1289 | neurodegenerative disease | ZFIN:ZDB-GENE-040219-1 | Danio rerio (zebrafish) | 403143 | sarm1 |
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| DOID:0112361 | spondylocostal dysostosis 3 | FB:FBgn0011591 | Drosophila melanogaster (fruit fly) | 40314 | fng | CG10580 |
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| DOID:6432 | pulmonary hypertension | ZFIN:ZDB-GENE-040218-2 | Danio rerio (zebrafish) | 403130 | has1 |
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| DOID:1168 | familial hyperlipidemia | ZFIN:ZDB-GENE-040718-68 | Danio rerio (zebrafish) | 403070 | rgn |
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| DOID:10534 | stomach cancer | ZFIN:ZDB-GENE-040718-68 | Danio rerio (zebrafish) | 403070 | rgn |
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| DOID:684 | hepatocellular carcinoma | ZFIN:ZDB-GENE-040718-68 | Danio rerio (zebrafish) | 403070 | rgn |
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| DOID:0080561 | congenital disorder of glycosylation Ii | ZFIN:ZDB-GENE-060502-2 | Danio rerio (zebrafish) | 403068 | alg2 |
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| DOID:0110669 | congenital myasthenic syndrome 14 | ZFIN:ZDB-GENE-060502-2 | Danio rerio (zebrafish) | 403068 | alg2 |
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| DOID:0060256 | Dowling-Degos disease | ZFIN:ZDB-GENE-040303-2 | Danio rerio (zebrafish) | 403029 | pofut1 |
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| DOID:0110366 | retinitis pigmentosa 33 | Xenbase:XB-GENE-941048 | Xenopus tropicalis (tropical clawed frog) | 402789 | st3gal3 |
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| DOID:10584 | retinitis pigmentosa | Xenbase:XB-GENE-941048 | Xenopus tropicalis (tropical clawed frog) | 402789 | st3gal3 |
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| DOID:0080414 | developmental and epileptic encephalopathy 15 | Xenbase:XB-GENE-941048 | Xenopus tropicalis (tropical clawed frog) | 402789 | st3gal3 |
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| DOID:0081180 | autosomal recessive intellectual developmental disorder 12 | Xenbase:XB-GENE-941048 | Xenopus tropicalis (tropical clawed frog) | 402789 | st3gal3 |
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