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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:2986 | IgA glomerulonephritis | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:2747 | glycogen storage disease | HGNC:4699 | Homo sapiens (human) | 2992 | GYG1 |
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| DOID:10024 | migraine with aura | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:0112223 | developmental and epileptic encephalopathy 89 | HGNC:4092 | Homo sapiens (human) | 2571 | GAD1 |
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| DOID:0060576 | 3MC syndrome 2 | HGNC:17213 | Homo sapiens (human) | 78989 | COLEC11 |
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| DOID:2957 | pulmonary tuberculosis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:2367 | neuroaxonal dystrophy | HGNC:9039 | Homo sapiens (human) | 8398 | PLA2G6 |
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| DOID:10211 | cholelithiasis | HGNC:2593 | Homo sapiens (human) | 1586 | CYP17A1 |
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| DOID:2228 | thrombocytosis | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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| DOID:1612 | breast cancer | HGNC:11377 | Homo sapiens (human) | 6783 | SULT1E1 |
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| DOID:0050546 | congenital adrenal insufficiency | HGNC:2590 | Homo sapiens (human) | 1583 | CYP11A1 |
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| DOID:8499 | night blindness | HGNC:8082 | Homo sapiens (human) | 60506 | NYX |
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| DOID:8692 | myeloid leukemia | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:0111411 | exudative vitreoretinopathy 4 | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:0080721 | calvarial doughnut lesions with bone fragility | HGNC:28395 | Homo sapiens (human) | 166929 | SGMS2 |
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| DOID:3146 | lipid metabolism disorder | HGNC:9232 | Homo sapiens (human) | 5465 | PPARA |
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| DOID:3905 | lung carcinoma | HGNC:2602 | Homo sapiens (human) | 1591 | CYP24A1 |
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| DOID:6543 | acne | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:3805 | porokeratosis | HGNC:3631 | Homo sapiens (human) | 2224 | FDPS |
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| DOID:61 | mitral valve disease | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:10892 | hypospadias | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:0110794 | hereditary spastic paraplegia 42 | HGNC:95 | Homo sapiens (human) | 9197 | SLC33A1 |
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| DOID:2986 | IgA glomerulonephritis | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
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| DOID:2394 | ovarian cancer | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:4372 | intracranial embolism | HGNC:6344 | Homo sapiens (human) | 9365 | KL |
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