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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:3328 | temporal lobe epilepsy | HGNC:7956 | Homo sapiens (human) | 4886 | NPY1R |
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| DOID:809 | cocaine abuse | HGNC:7956 | Homo sapiens (human) | 4886 | NPY1R |
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| DOID:1824 | status epilepticus | HGNC:8021 | Homo sapiens (human) | 4907 | NT5E |
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| DOID:0111582 | hereditary arterial and articular multiple calcification syndrome | HGNC:8021 | Homo sapiens (human) | 4907 | NT5E |
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| DOID:0080411 | familial adenomatous polyposis 3 | HGNC:8028 | Homo sapiens (human) | 4913 | NTHL1 |
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| DOID:0111235 | congenital muscular dystrophy-dystroglycanopathy type A12 | ZFIN:ZDB-GENE-041114-119 | Danio rerio (zebrafish) | 492773 | pomk |
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| DOID:10908 | hydrocephalus | ZFIN:ZDB-GENE-041114-119 | Danio rerio (zebrafish) | 492773 | pomk |
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| DOID:0112381 | muscular dystrophy-dystroglycanopathy type C12 | ZFIN:ZDB-GENE-041114-119 | Danio rerio (zebrafish) | 492773 | pomk |
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| DOID:206 | hereditary multiple exostoses | Xenbase:XB-GENE-855819 | Xenopus tropicalis (tropical clawed frog) | 493398 | extl3 |
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| DOID:206 | hereditary multiple exostoses | ZFIN:ZDB-GENE-041124-3 | Danio rerio (zebrafish) | 493780 | ext2 |
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| DOID:206 | hereditary multiple exostoses | ZFIN:ZDB-GENE-041124-2 | Danio rerio (zebrafish) | 493783 | extl3 |
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| DOID:612 | primary immunodeficiency disease | HGNC:8086 | Homo sapiens (human) | 4938 | OAS1 |
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| DOID:0111453 | 2-aminoadipic 2-oxoadipic aciduria | ZFIN:ZDB-GENE-041212-44 | Danio rerio (zebrafish) | 494076 | dhtkd1 |
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| DOID:0110170 | Charcot-Marie-Tooth disease axonal type 2Q | ZFIN:ZDB-GENE-041212-44 | Danio rerio (zebrafish) | 494076 | dhtkd1 |
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| DOID:0060227 | Adams-Oliver syndrome | RGD:1359357 | Rattus norvegicus (Norway rat) | 494219 | Eogt |
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| DOID:0080520 | Tn polyagglutination syndrome | Xenbase:XB-GENE-941235 | Xenopus laevis (African clawed frog) | 495031 | c1galt1c1.L |
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| DOID:12554 | hemolytic-uremic syndrome | Xenbase:XB-GENE-941235 | Xenopus laevis (African clawed frog) | 495031 | c1galt1c1.L |
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| DOID:1056 | oculocerebrorenal syndrome | HGNC:8108 | Homo sapiens (human) | 4952 | OCRL |
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| DOID:0050699 | Dent disease | HGNC:8108 | Homo sapiens (human) | 4952 | OCRL |
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| DOID:0050453 | lissencephaly | Xenbase:XB-GENE-959859 | Xenopus laevis (African clawed frog) | 495292 | pomgnt1.S |
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| DOID:9884 | muscular dystrophy | Xenbase:XB-GENE-959859 | Xenopus laevis (African clawed frog) | 495292 | pomgnt1.S |
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| DOID:0050560 | Walker-Warburg syndrome | Xenbase:XB-GENE-959859 | Xenopus laevis (African clawed frog) | 495292 | pomgnt1.S |
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| DOID:0110292 | autosomal recessive limb-girdle muscular dystrophy type 2O | Xenbase:XB-GENE-959859 | Xenopus laevis (African clawed frog) | 495292 | pomgnt1.S |
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| DOID:10584 | retinitis pigmentosa | Xenbase:XB-GENE-959859 | Xenopus laevis (African clawed frog) | 495292 | pomgnt1.S |
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| DOID:0112378 | muscular dystrophy-dystroglycanopathy type B3 | Xenbase:XB-GENE-959859 | Xenopus laevis (African clawed frog) | 495292 | pomgnt1.S |
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