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GlyTouCan
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:0080217 | lysosomal acid lipase deficiency | HGNC:6617 | Homo sapiens (human) | 3988 | LIPA |
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| DOID:14497 | Wolman disease | HGNC:6617 | Homo sapiens (human) | 3988 | LIPA |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | Xenbase:XB-GENE-6078761 | Xenopus laevis (African clawed frog) | 398800 | dgat2.L |
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| DOID:2018 | hyperinsulinism | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:2237 | hepatitis | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:1168 | familial hyperlipidemia | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:1312 | focal segmental glomerulosclerosis | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:783 | end stage renal disease | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:557 | kidney disease | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:10652 | Alzheimer's disease | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:341 | peripheral vascular disease | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:1459 | hypothyroidism | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:11801 | protein-energy malnutrition | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:9970 | obesity | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:326 | ischemia | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:13809 | familial combined hyperlipidemia | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:3393 | coronary artery disease | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:1184 | nephrotic syndrome | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:0081326 | oxoglutarate dehydrogenase deficiency | Xenbase:XB-GENE-1010765 | Xenopus laevis (African clawed frog) | 399021 | ogdh.S |
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| DOID:3371 | chondrosarcoma | Xenbase:XB-GENE-867536 | Xenopus laevis (African clawed frog) | 399115 | ext1.S |
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| DOID:206 | hereditary multiple exostoses | Xenbase:XB-GENE-867536 | Xenopus laevis (African clawed frog) | 399115 | ext1.S |
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| DOID:5844 | myocardial infarction | Xenbase:XB-GENE-484957 | Xenopus laevis (African clawed frog) | 399170 | akt1.S |
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| DOID:7575 | pancreatic intraductal papillary-mucinous neoplasm | Xenbase:XB-GENE-484957 | Xenopus laevis (African clawed frog) | 399170 | akt1.S |
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