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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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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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:12849 | autistic disorder | HGNC:5173 | Homo sapiens (human) | 3265 | HRAS |
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| DOID:5419 | schizophrenia | HGNC:1939 | Homo sapiens (human) | 10752 | CHL1 |
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| DOID:0110204 | Charcot-Marie-Tooth disease recessive intermediate B | HGNC:6215 | Homo sapiens (human) | 3735 | KARS1 |
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| DOID:8398 | osteoarthritis | HGNC:11891 | Homo sapiens (human) | 7123 | CLEC3B |
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| DOID:12129 | bulimia nervosa | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:0050861 | colorectal adenocarcinoma | HGNC:5331 | Homo sapiens (human) | 64127 | NOD2 |
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| DOID:3121 | gallbladder cancer | HGNC:603 | Homo sapiens (human) | 338 | APOB |
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| DOID:0080661 | nonsyndromic aplasia cutis congenita | HGNC:23505 | Homo sapiens (human) | 9790 | BMS1 |
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| DOID:0060944 | episodic kinesigenic dyskinesia 3 | HGNC:28497 | Homo sapiens (human) | 256472 | TMEM151A |
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| DOID:12206 | dengue hemorrhagic fever | HGNC:11050 | Homo sapiens (human) | 6532 | SLC6A4 |
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| DOID:2986 | IgA glomerulonephritis | HGNC:23282 | Homo sapiens (human) | 200958 | MUC20 |
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| DOID:3393 | coronary artery disease | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:12930 | dilated cardiomyopathy | HGNC:5724 | Homo sapiens (human) | 3516 | RBPJ |
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| DOID:0070525 | peeling skin syndrome 6 | HGNC:33276 | Homo sapiens (human) | 388698 | FLG2 |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:17601 | Homo sapiens (human) | 57863 | CADM3 |
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| DOID:7148 | rheumatoid arthritis | HGNC:1324 | Homo sapiens (human) | 721 | C4B |
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| DOID:2987 | familial mediterranean fever | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:0060209 | amyotrophic lateral sclerosis type 18 | HGNC:8881 | Homo sapiens (human) | 5216 | PFN1 |
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| DOID:11695 | portal vein thrombosis | HGNC:5465 | Homo sapiens (human) | 3480 | IGF1R |
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| DOID:0070342 | adult-onset type II citrullinemia | HGNC:10983 | Homo sapiens (human) | 10165 | SLC25A13 |
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| DOID:3969 | thyroid gland papillary carcinoma | HGNC:11825 | Homo sapiens (human) | 7080 | NKX2-1 |
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| DOID:0090076 | hypogonadotropic hypogonadism 18 with or without anosmia | HGNC:17616 | Homo sapiens (human) | 54756 | IL17RD |
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| DOID:783 | end stage renal disease | HGNC:10720 | Homo sapiens (human) | 6402 | SELL |
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| DOID:5082 | liver cirrhosis | HGNC:4886 | Homo sapiens (human) | 3077 | HFE |
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| DOID:1825 | childhood absence epilepsy | RGD:2244 | Rattus norvegicus (Norway rat) | 25398 | Cacna1a |
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