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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:0090032 | Silverman-Handmaker type dyssegmental dysplasia | HGNC:5273 | Homo sapiens (human) | 3339 | HSPG2 |
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| DOID:0060770 | dextro-looped transposition of the great arteries | HGNC:5273 | Homo sapiens (human) | 3339 | HSPG2 |
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| DOID:3407 | carotid artery disease | HGNC:5273 | Homo sapiens (human) | 3339 | HSPG2 |
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| DOID:4195 | hyperglycemia | HGNC:5273 | Homo sapiens (human) | 3339 | HSPG2 |
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| DOID:13481 | thanatophoric dysplasia | HGNC:5273 | Homo sapiens (human) | 3339 | HSPG2 |
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| DOID:0090005 | Schwartz-Jampel syndrome 1 | HGNC:5273 | Homo sapiens (human) | 3339 | HSPG2 |
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| DOID:1059 | intellectual disability | HGNC:7680 | Homo sapiens (human) | 3340 | NDST1 |
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| DOID:11198 | DiGeorge syndrome | HGNC:7680 | Homo sapiens (human) | 3340 | NDST1 |
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| DOID:14227 | azoospermia | HGNC:7680 | Homo sapiens (human) | 3340 | NDST1 |
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| DOID:0081210 | autosomal recessive intellectual developmental disorder 46 | HGNC:7680 | Homo sapiens (human) | 3340 | NDST1 |
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| DOID:12716 | newborn respiratory distress syndrome | HGNC:7680 | Homo sapiens (human) | 3340 | NDST1 |
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| DOID:0060041 | autism spectrum disorder | HGNC:7680 | Homo sapiens (human) | 3340 | NDST1 |
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| DOID:3827 | congenital diaphragmatic hernia | HGNC:7680 | Homo sapiens (human) | 3340 | NDST1 |
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| DOID:0050570 | congenital disorder of glycosylation type I | ZFIN:ZDB-GENE-030131-6093 | Danio rerio (zebrafish) | 334161 | alg1 |
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| DOID:0080563 | congenital disorder of glycosylation Ik | ZFIN:ZDB-GENE-030131-6093 | Danio rerio (zebrafish) | 334161 | alg1 |
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| DOID:5212 | congenital disorder of glycosylation | ZFIN:ZDB-GENE-030131-6093 | Danio rerio (zebrafish) | 334161 | alg1 |
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| DOID:0060227 | Adams-Oliver syndrome | FB:FBgn0264672 | Drosophila melanogaster (fruit fly) | 33424 | Eogt | CG9867 |
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| DOID:583 | hemolytic anemia | FB:FBgn0250906 | Drosophila melanogaster (fruit fly) | 33461 | Pgk |
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| DOID:162 | cancer | FB:FBgn0250906 | Drosophila melanogaster (fruit fly) | 33461 | Pgk |
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| DOID:0111933 | phosphoglycerate kinase 1 deficiency | FB:FBgn0250906 | Drosophila melanogaster (fruit fly) | 33461 | Pgk |
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| DOID:14330 | Parkinson's disease | FB:FBgn0250906 | Drosophila melanogaster (fruit fly) | 33461 | Pgk |
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| DOID:1793 | pancreatic cancer | FB:FBgn0031491 | Drosophila melanogaster (fruit fly) | 33512 | α4GT1 | CG17223 |
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| DOID:1793 | pancreatic cancer | FB:FBgn0031491 | Drosophila melanogaster (fruit fly) | 33512 | alpha4GT1 | CG17223 |
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| DOID:224 | transient cerebral ischemia | FB:FBgn0010247 | Drosophila melanogaster (fruit fly) | 3355109 | Parp1 |
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| DOID:848 | arthritis | FB:FBgn0010247 | Drosophila melanogaster (fruit fly) | 3355109 | Parp1 |
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