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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:0050865 | tongue squamous cell carcinoma | RGD:3073 | Rattus norvegicus (Norway rat) | 50567 | Slc3a2 |
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| DOID:0080202 | adenoid cystic carcinoma | RGD:3073 | Rattus norvegicus (Norway rat) | 50567 | Slc3a2 |
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| DOID:0080855 | Parkinsonism | RGD:620351 | Rattus norvegicus (Norway rat) | 50686 | Gsk3a |
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| DOID:332 | amyotrophic lateral sclerosis | RGD:620351 | Rattus norvegicus (Norway rat) | 50686 | Gsk3a |
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| DOID:3911 | progeria | MGI:1354161 | Mus musculus (house mouse) | 50721 | Sirt6 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | MGI:1354161 | Mus musculus (house mouse) | 50721 | Sirt6 |
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| DOID:224 | transient cerebral ischemia | MGI:1354161 | Mus musculus (house mouse) | 50721 | Sirt6 |
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| DOID:9970 | obesity | MGI:1354161 | Mus musculus (house mouse) | 50721 | Sirt6 |
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| DOID:0090075 | hypogonadotropic hypogonadism 15 with or without anosmia | MGI:1354958 | Mus musculus (house mouse) | 50785 | Hs6st1 |
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| DOID:0111843 | Paganini-Miozzo syndrome | MGI:1354959 | Mus musculus (house mouse) | 50786 | Hs6st2 |
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| DOID:3659 | sialuria | MGI:1354951 | Mus musculus (house mouse) | 50798 | Gne |
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| DOID:0080718 | GNE myopathy | MGI:1354951 | Mus musculus (house mouse) | 50798 | Gne |
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| DOID:4137 | common bile duct disease | MGI:1354721 | Mus musculus (house mouse) | 50799 | Slc25a13 |
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| DOID:1852 | intrahepatic cholestasis | MGI:1354721 | Mus musculus (house mouse) | 50799 | Slc25a13 |
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| DOID:0070342 | adult-onset type II citrullinemia | MGI:1354721 | Mus musculus (house mouse) | 50799 | Slc25a13 |
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| DOID:0070341 | neonatal-onset type II citrullinemia | MGI:1354721 | Mus musculus (house mouse) | 50799 | Slc25a13 |
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| DOID:9273 | citrullinemia | MGI:1354721 | Mus musculus (house mouse) | 50799 | Slc25a13 |
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| DOID:0060292 | X-linked chondrodysplasia punctata 1 | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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| DOID:0111822 | CHILD syndrome | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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| DOID:0111898 | CK syndrome | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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| DOID:12305 | Bloch-Sulzberger syndrome | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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| DOID:162 | cancer | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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| DOID:3651 | pyruvate carboxylase deficiency disease | HGNC:8636 | Homo sapiens (human) | 5091 | PC |
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| DOID:9252 | amino acid metabolic disorder | HGNC:8653 | Homo sapiens (human) | 5095 | PCCA |
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| DOID:14701 | propionic acidemia | HGNC:8653 | Homo sapiens (human) | 5095 | PCCA |
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