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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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▲ | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0050439 | Usher syndrome | HGNC:12601 | Homo sapiens (human) | 7399 | USH2A |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:4396 | Homo sapiens (human) | 2782 | GNB1 |
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| DOID:0080784 | urinary tract infection | HGNC:5233 | Homo sapiens (human) | 3304 | HSPA1B |
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| DOID:0080016 | spina bifida | HGNC:587 | Homo sapiens (human) | 328 | APEX1 |
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| DOID:14330 | Parkinson's disease | HGNC:1963 | Homo sapiens (human) | 1142 | CHRNB3 |
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| DOID:0050156 | idiopathic pulmonary fibrosis | HGNC:11730 | Homo sapiens (human) | 7015 | TERT |
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| DOID:4362 | cervical cancer | HGNC:7155 | Homo sapiens (human) | 4312 | MMP1 |
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| DOID:12399 | pathological gambling | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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| DOID:1596 | depressive disorder | HGNC:8154 | Homo sapiens (human) | 4986 | OPRK1 |
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| DOID:0060309 | syndromic X-linked intellectual disability | HGNC:2745 | Homo sapiens (human) | 1654 | DDX3X |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:3023 | Homo sapiens (human) | 1813 | DRD2 |
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| DOID:0111233 | congenital muscular dystrophy-dystroglycanopathy A14 | HGNC:22932 | Homo sapiens (human) | 29925 | GMPPB |
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| DOID:0070058 | Helsmoortel-Van Der Aa Syndrome | HGNC:15766 | Homo sapiens (human) | 23394 | ADNP |
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| DOID:12361 | Graves' disease | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:10839 | Homo sapiens (human) | 6462 | SHBG |
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| DOID:0060496 | respiratory allergy | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:3393 | coronary artery disease | HGNC:336 | Homo sapiens (human) | 185 | AGTR1 |
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| DOID:12205 | dengue disease | HGNC:3616 | Homo sapiens (human) | 2212 | FCGR2A |
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| DOID:0111161 | Crouzon syndrome-acanthosis nigricans syndrome | HGNC:3690 | Homo sapiens (human) | 2261 | FGFR3 |
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| DOID:0110042 | Alzheimer's disease 3 | HGNC:613 | Homo sapiens (human) | 348 | APOE |
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| DOID:0080488 | mucolipidosis | HGNC:7758 | Homo sapiens (human) | 4758 | NEU1 |
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| DOID:0060041 | autism spectrum disorder | HGNC:947 | Homo sapiens (human) | 10458 | BAIAP2 |
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| DOID:0060558 | lethal congenital contracture syndrome | HGNC:18591 | Homo sapiens (human) | 91754 | NEK9 |
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| DOID:0080353 | X-linked recessive hypophosphatemic rickets | HGNC:2023 | Homo sapiens (human) | 1184 | CLCN5 |
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| DOID:0080272 | nephrotic syndrome type 16 | HGNC:29300 | Homo sapiens (human) | 25959 | KANK2 |
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