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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:9970 | obesity | RGD:2797 | Rattus norvegicus (Norway rat) | 25059 | Hk2 |
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| DOID:1561 | cognitive disorder | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:0060233 | cardiofaciocutaneous syndrome | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:0050560 | Walker-Warburg syndrome | MGI:1915523 | Mus musculus (house mouse) | 68273 | Pomgnt1 |
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| DOID:14118 | familial lipoprotein lipase deficiency | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
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| DOID:850 | lung disease | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:1909 | melanoma | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:10763 | hypertension | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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| DOID:9352 | type 2 diabetes mellitus | RGD:2644 | Rattus norvegicus (Norway rat) | 25634 | G6pc1 |
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| DOID:9452 | steatotic liver disease | RGD:3369 | Rattus norvegicus (Norway rat) | 25747 | Ppara |
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| DOID:9452 | steatotic liver disease | HGNC:9232 | Homo sapiens (human) | 5465 | PPARA |
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| DOID:783 | end stage renal disease | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0090031 | D-bifunctional protein deficiency | HGNC:5213 | Homo sapiens (human) | 3295 | HSD17B4 |
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| DOID:3633 | beta-mannosidosis | MGI:88175 | Mus musculus (house mouse) | 110173 | Manba |
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| DOID:2843 | long QT syndrome | RGD:621503 | Rattus norvegicus (Norway rat) | 84020 | Kcnq1 |
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| DOID:0050570 | congenital disorder of glycosylation type I | MGI:97075 | Mus musculus (house mouse) | 110119 | Mpi |
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| DOID:684 | hepatocellular carcinoma | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:3012 | Li-Fraumeni syndrome | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:9352 | type 2 diabetes mellitus | MGI:104663 | Mus musculus (house mouse) | 16846 | Lep |
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| DOID:8677 | perinatal necrotizing enterocolitis | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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| DOID:206 | hereditary multiple exostoses | MGI:108050 | Mus musculus (house mouse) | 14043 | Ext2 |
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| DOID:10763 | hypertension | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0090129 | carnitine palmitoyltransferase I deficiency | MGI:1098296 | Mus musculus (house mouse) | 12894 | Cpt1a |
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| DOID:1612 | breast cancer | MGI:98834 | Mus musculus (house mouse) | 22059 | Trp53 |
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| DOID:10763 | hypertension | HGNC:2642 | Homo sapiens (human) | 1579 | CYP4A11 |
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