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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:0081243 | rhizomelic chondrodysplasia punctate type 4 | HGNC:26222 | Homo sapiens (human) | 84188 | FAR1 |
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| DOID:1380 | endometrial cancer | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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| DOID:670 | amphetamine abuse | HGNC:7956 | Homo sapiens (human) | 4886 | NPY1R |
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| DOID:2256 | osteochondrodysplasia | HGNC:1971 | Homo sapiens (human) | 9469 | CHST3 |
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| DOID:5419 | schizophrenia | HGNC:6051 | Homo sapiens (human) | 3613 | IMPA2 |
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| DOID:0070260 | congenital disorder of glycosylation type IIh | HGNC:18623 | Homo sapiens (human) | 84342 | COG8 |
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| DOID:705 | Leber hereditary optic neuropathy | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0070519 | early-onset vitamin B6-dependent epilepsy 4 | HGNC:877 | Homo sapiens (human) | 501 | ALDH7A1 |
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| DOID:0080501 | GM1 gangliosidosis type 2 | HGNC:4298 | Homo sapiens (human) | 2720 | GLB1 |
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| DOID:9119 | acute myeloid leukemia | HGNC:2615 | Homo sapiens (human) | 1555 | CYP2B6 |
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| DOID:0070433 | hyperphosphatasia with impaired intellectual development syndrome 1 | HGNC:26031 | Homo sapiens (human) | 55650 | PIGV |
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| DOID:7693 | abdominal aortic aneurysm | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
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| DOID:0111061 | familial hypobetalipoproteinemia 2 | HGNC:491 | Homo sapiens (human) | 27329 | ANGPTL3 |
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| DOID:988 | mitral valve prolapse | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:1852 | intrahepatic cholestasis | HGNC:18324 | Homo sapiens (human) | 80270 | HSD3B7 |
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| DOID:0090139 | cortisone reductase deficiency | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:1070 | primary open angle glaucoma | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:10763 | hypertension | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
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| DOID:4810 | cerebrotendinous xanthomatosis | HGNC:2605 | Homo sapiens (human) | 1593 | CYP27A1 |
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| DOID:1324 | lung cancer | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:0112376 | muscular dystrophy-dystroglycanopathy type B15 | HGNC:3007 | Homo sapiens (human) | 54344 | DPM3 |
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| DOID:8577 | ulcerative colitis | HGNC:2602 | Homo sapiens (human) | 1591 | CYP24A1 |
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| DOID:14695 | galactokinase deficiency | HGNC:4118 | Homo sapiens (human) | 2584 | GALK1 |
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| DOID:4661 | multiple chemical sensitivity | HGNC:2621 | Homo sapiens (human) | 1557 | CYP2C19 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:6080 | Homo sapiens (human) | 3636 | INPPL1 |
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