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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:6000 | congestive heart failure | MGI:109354 | Mus musculus (house mouse) | 22228 | Ucp2 |
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| DOID:13603 | obstructive jaundice | RGD:3932 | Rattus norvegicus (Norway rat) | 54315 | Ucp2 |
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| DOID:1459 | hypothyroidism | RGD:3932 | Rattus norvegicus (Norway rat) | 54315 | Ucp2 |
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| DOID:9743 | diabetic neuropathy | RGD:3932 | Rattus norvegicus (Norway rat) | 54315 | Ucp2 |
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| DOID:12858 | Huntington's disease | RGD:3932 | Rattus norvegicus (Norway rat) | 54315 | Ucp2 |
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| DOID:224 | transient cerebral ischemia | MGI:109354 | Mus musculus (house mouse) | 22228 | Ucp2 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | RGD:3932 | Rattus norvegicus (Norway rat) | 54315 | Ucp2 |
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| DOID:1094 | attention deficit hyperactivity disorder | HGNC:17223 | Homo sapiens (human) | 10090 | UST |
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| DOID:653 | purine-pyrimidine metabolic disorder | SGD:S000000747 | Saccharomyces cerevisiae S288C | 856692 | URA3 |
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| DOID:0050833 | orotic aciduria | SGD:S000000747 | Saccharomyces cerevisiae S288C | 856692 | URA3 |
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| DOID:3525 | middle cerebral artery infarction | HGNC:12576 | Homo sapiens (human) | 7378 | UPP1 |
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| DOID:0060759 | immunodeficiency with hyper IgM type 5 | SGD:S000004483 | Saccharomyces cerevisiae S288C | 854987 | UNG1 |
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| DOID:11702 | dysgammaglobulinemia | SGD:S000004483 | Saccharomyces cerevisiae S288C | 854987 | UNG1 |
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| DOID:0060759 | immunodeficiency with hyper IgM type 5 | HGNC:12572 | Homo sapiens (human) | 7374 | UNG |
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| DOID:11702 | dysgammaglobulinemia | HGNC:12572 | Homo sapiens (human) | 7374 | UNG |
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| DOID:653 | purine-pyrimidine metabolic disorder | HGNC:12563 | Homo sapiens (human) | 7372 | UMPS |
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| DOID:0050833 | orotic aciduria | HGNC:12563 | Homo sapiens (human) | 7372 | UMPS |
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| DOID:0060062 | familial juvenile hyperuricemic nephropathy | HGNC:12559 | Homo sapiens (human) | 7369 | UMOD |
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| DOID:557 | kidney disease | HGNC:12559 | Homo sapiens (human) | 7369 | UMOD |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:12541 | Homo sapiens (human) | 54600 | UGT1A9 |
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| DOID:4947 | cholangiocarcinoma | HGNC:12541 | Homo sapiens (human) | 54600 | UGT1A9 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:12540 | Homo sapiens (human) | 54576 | UGT1A8 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:12539 | Homo sapiens (human) | 54577 | UGT1A7 |
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| DOID:4988 | alcoholic pancreatitis | HGNC:12539 | Homo sapiens (human) | 54577 | UGT1A7 |
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| DOID:1793 | pancreatic cancer | HGNC:12539 | Homo sapiens (human) | 54577 | UGT1A7 |
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