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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:10534 | stomach cancer | RGD:3560 | Rattus norvegicus (Norway rat) | 25106 | Rgn |
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| DOID:684 | hepatocellular carcinoma | MGI:108024 | Mus musculus (house mouse) | 19733 | Rgn |
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| DOID:0060036 | intrinsic cardiomyopathy | FB:FBgn0002622 | Drosophila melanogaster (fruit fly) | 42761 | RpS3 |
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| DOID:0111239 | congenital muscular dystrophy-dystroglycanopathy type A10 | MGI:2384919 | Mus musculus (house mouse) | 216395 | Rxylt1 |
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| DOID:0050560 | Walker-Warburg syndrome | MGI:2384919 | Mus musculus (house mouse) | 216395 | Rxylt1 |
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| DOID:0050560 | Walker-Warburg syndrome | RGD:1309356 | Rattus norvegicus (Norway rat) | 299841 | Rxylt1 |
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| DOID:0111239 | congenital muscular dystrophy-dystroglycanopathy type A10 | RGD:1309356 | Rattus norvegicus (Norway rat) | 299841 | Rxylt1 |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:17074 | Homo sapiens (human) | 23098 | SARM1 |
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| DOID:1289 | neurodegenerative disease | HGNC:17074 | Homo sapiens (human) | 23098 | SARM1 |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | HGNC:10571 | Homo sapiens (human) | 6319 | SCD |
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| DOID:397 | restrictive cardiomyopathy | HGNC:10571 | Homo sapiens (human) | 6319 | SCD |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:10571 | Homo sapiens (human) | 6319 | SCD |
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| DOID:305 | carcinoma | HGNC:10571 | Homo sapiens (human) | 6319 | SCD |
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| DOID:2018 | hyperinsulinism | HGNC:10571 | Homo sapiens (human) | 6319 | SCD |
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| DOID:0112160 | autosomal dominant nonsyndromic deafness 79 | HGNC:21088 | Homo sapiens (human) | 79966 | SCD5 |
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| DOID:397 | restrictive cardiomyopathy | HGNC:21088 | Homo sapiens (human) | 79966 | SCD5 |
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| DOID:9970 | obesity | HGNC:10606 | Homo sapiens (human) | 6342 | SCP2 |
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| DOID:905 | Zellweger syndrome | HGNC:10606 | Homo sapiens (human) | 6342 | SCP2 |
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| DOID:9970 | obesity | HGNC:10658 | Homo sapiens (human) | 6382 | SDC1 |
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| DOID:4195 | hyperglycemia | HGNC:10658 | Homo sapiens (human) | 6382 | SDC1 |
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| DOID:1168 | familial hyperlipidemia | HGNC:10658 | Homo sapiens (human) | 6382 | SDC1 |
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| DOID:8567 | Hodgkin's lymphoma | HGNC:10658 | Homo sapiens (human) | 6382 | SDC1 |
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| DOID:576 | proteinuria | HGNC:10658 | Homo sapiens (human) | 6382 | SDC1 |
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| DOID:5844 | myocardial infarction | HGNC:10658 | Homo sapiens (human) | 6382 | SDC1 |
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| DOID:3910 | lung adenocarcinoma | HGNC:10658 | Homo sapiens (human) | 6382 | SDC1 |
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