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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:0081427 | autosomal recessive distal hereditary motor neuronopathy 8 | RGD:3734 | Rattus norvegicus (Norway rat) | 24788 | Sord |
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| DOID:0081427 | autosomal recessive distal hereditary motor neuronopathy 8 | SGD:S000002405 | Saccharomyces cerevisiae S288C | 851351 | SOR2 |
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| DOID:0081427 | autosomal recessive distal hereditary motor neuronopathy 8 | SGD:S000004060 | Saccharomyces cerevisiae S288C | 850759 | XYL2 |
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| DOID:0081427 | autosomal recessive distal hereditary motor neuronopathy 8 | SGD:S000003920 | Saccharomyces cerevisiae S288C | 853624 | SOR1 |
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| DOID:0081427 | autosomal recessive distal hereditary motor neuronopathy 8 | MGI:98266 | Mus musculus (house mouse) | 20322 | Sord |
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| DOID:0081427 | autosomal recessive distal hereditary motor neuronopathy 8 | HGNC:11184 | Homo sapiens (human) | 6652 | SORD |
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| DOID:0070129 | autosomal recessive cutis laxa type IID | Xenbase:XB-GENE-990439 | Xenopus tropicalis (tropical clawed frog) | 407846 | st6gal2 |
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| DOID:0070129 | autosomal recessive cutis laxa type IID | HGNC:851 | Homo sapiens (human) | 523 | ATP6V1A |
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| DOID:0070134 | autosomal recessive cutis laxa type IIA | HGNC:18481 | Homo sapiens (human) | 23545 | ATP6V0A2 |
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| DOID:0060718 | autosomal recessive congenital ichthyosis 9 | HGNC:23752 | Homo sapiens (human) | 204219 | CERS3 |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | HGNC:8957 | Homo sapiens (human) | 5277 | PIGA |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | WB:WBGene00008431 | Caenorhabditis elegans | 174386 | piga-1 |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | ZFIN:ZDB-GENE-040426-1086 | Danio rerio (zebrafish) | 791759 | piga |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | MGI:99461 | Mus musculus (house mouse) | 18700 | Piga |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | HGNC:9491 | Homo sapiens (human) | 5652 | PRSS8 |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | Xenbase:XB-GENE-996765 | Xenopus tropicalis (tropical clawed frog) | 100158632 | piga |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | FB:FBgn0034270 | Drosophila melanogaster (fruit fly) | 37020 | PIG-A |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | RGD:1589723 | Rattus norvegicus (Norway rat) | 363464 | Piga |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | SGD:S000006096 | Saccharomyces cerevisiae S288C | 855928 | SPT14 |
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| DOID:0060710 | autosomal recessive congenital ichthyosis 2 | HGNC:430 | Homo sapiens (human) | 242 | ALOX12B |
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| DOID:0080258 | autosomal recessive congenital ichthyosis 14 | HGNC:11459 | Homo sapiens (human) | 6820 | SULT2B1 |
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| DOID:898 | autosomal dominant polycystic kidney disease | HGNC:9009 | Homo sapiens (human) | 5311 | PKD2 |
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| DOID:898 | autosomal dominant polycystic kidney disease | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:898 | autosomal dominant polycystic kidney disease | HGNC:9008 | Homo sapiens (human) | 5310 | PKD1 |
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| DOID:898 | autosomal dominant polycystic kidney disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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