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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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Repository for lectin-assisted multimodality data
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MIRAGE
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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▼ | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0070187 | Y-linked spermatogenic failure 2 | HGNC:12633 | Homo sapiens (human) | 8287 | USP9Y |
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| DOID:1612 | breast cancer | HGNC:3528 | Homo sapiens (human) | 2159 | F10 |
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| DOID:0060001 | withdrawal disorder | HGNC:17071 | Homo sapiens (human) | 23081 | KDM4C |
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| DOID:0050562 | West syndrome | HGNC:6930 | Homo sapiens (human) | 4158 | MC2R |
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| DOID:0070380 | developmental and epileptic encephalopathy 85 | HGNC:11111 | Homo sapiens (human) | 8243 | SMC1A |
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| DOID:0070223 | progressive familial intrahepatic cholestasis 3 | HGNC:45 | Homo sapiens (human) | 5244 | ABCB4 |
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| DOID:11054 | urinary bladder cancer | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:0081220 | autosomal recessive intellectual developmental disorder 58 | HGNC:18248 | Homo sapiens (human) | 55250 | ELP2 |
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| DOID:0070215 | familial hyperinsulinemic hypoglycemia 4 | HGNC:4799 | Homo sapiens (human) | 3033 | HADH |
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| DOID:14557 | primary pulmonary hypertension | HGNC:9603 | Homo sapiens (human) | 5740 | PTGIS |
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| DOID:10652 | Alzheimer's disease | HGNC:6701 | Homo sapiens (human) | 4043 | LRPAP1 |
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| DOID:848 | arthritis | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:1612 | breast cancer | HGNC:3273 | Homo sapiens (human) | 8667 | EIF3H |
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| DOID:9253 | gastrointestinal stromal tumor | HGNC:10681 | Homo sapiens (human) | 6390 | SDHB |
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| DOID:0081109 | keratosis palmoplantaris striata 2 | HGNC:3052 | Homo sapiens (human) | 1832 | DSP |
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| DOID:0080199 | colorectal carcinoma | HGNC:6919 | Homo sapiens (human) | 8930 | MBD4 |
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| DOID:0080352 | X-linked chondrodysplasia punctata 2 | HGNC:3133 | Homo sapiens (human) | 10682 | EBP |
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| DOID:12918 | thromboangiitis obliterans | HGNC:4931 | Homo sapiens (human) | 3105 | HLA-A |
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| DOID:0060679 | catecholaminergic polymorphic ventricular tachycardia 5 | HGNC:12261 | Homo sapiens (human) | 10345 | TRDN |
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| DOID:10283 | prostate cancer | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:2569 | retinal drusen | HGNC:4883 | Homo sapiens (human) | 3075 | CFH |
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| DOID:0081128 | mandibuloacral dysplasia type A lipodystrophy | HGNC:6636 | Homo sapiens (human) | 4000 | LMNA |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:10914 | Homo sapiens (human) | 9990 | SLC12A6 |
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| DOID:0110289 | autosomal recessive limb-girdle muscular dystrophy type 2Y | HGNC:29456 | Homo sapiens (human) | 26092 | TOR1AIP1 |
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| DOID:9970 | obesity | HGNC:286 | Homo sapiens (human) | 154 | ADRB2 |
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