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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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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:9975 | cocaine dependence | HGNC:8153 | Homo sapiens (human) | 4985 | OPRD1 |
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| DOID:10159 | osteonecrosis | HGNC:19100 | Homo sapiens (human) | 149233 | IL23R |
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| DOID:13166 | allergic bronchopulmonary aspergillosis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:4450 | renal cell carcinoma | HGNC:393 | Homo sapiens (human) | 10000 | AKT3 |
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| DOID:0050741 | alcohol dependence | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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| DOID:0070303 | multiple epiphyseal dysplasia 1 | HGNC:2227 | Homo sapiens (human) | 1311 | COMP |
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| DOID:1827 | idiopathic generalized epilepsy | HGNC:6284 | Homo sapiens (human) | 3778 | KCNMA1 |
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| DOID:7575 | pancreatic intraductal papillary-mucinous neoplasm | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0070210 | hereditary lymphedema IA | HGNC:3767 | Homo sapiens (human) | 2324 | FLT4 |
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| DOID:3526 | cerebral infarction | HGNC:1181 | Homo sapiens (human) | 745 | MYRF |
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| DOID:0111098 | Fanconi anemia complementation group B | HGNC:3583 | Homo sapiens (human) | 2187 | FANCB |
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| DOID:13382 | megaloblastic anemia | HGNC:14604 | Homo sapiens (human) | 81693 | AMN |
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| DOID:0111527 | spinal muscular atrophy with progressive myoclonic epilepsy | HGNC:735 | Homo sapiens (human) | 427 | ASAH1 |
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| DOID:0050742 | nicotine dependence | HGNC:1959 | Homo sapiens (human) | 1138 | CHRNA5 |
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| DOID:0110965 | brachydactyly type A2 | HGNC:1069 | Homo sapiens (human) | 650 | BMP2 |
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| DOID:0111364 | Alzheimer's disease 9 | HGNC:37 | Homo sapiens (human) | 10347 | ABCA7 |
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| DOID:631 | fibromyalgia | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:0111123 | nephronophthisis 15 | HGNC:29182 | Homo sapiens (human) | 22897 | CEP164 |
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| DOID:9074 | systemic lupus erythematosus | HGNC:7067 | Homo sapiens (human) | 4261 | CIITA |
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| DOID:3312 | bipolar disorder | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:10534 | stomach cancer | HGNC:20185 | Homo sapiens (human) | 54916 | TMEM260 |
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| DOID:5683 | hereditary breast ovarian cancer syndrome | HGNC:1101 | Homo sapiens (human) | 675 | BRCA2 |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:13861 | Homo sapiens (human) | 11178 | LZTS1 |
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| DOID:0050564 | autosomal dominant nonsyndromic deafness | HGNC:2186 | Homo sapiens (human) | 1301 | COL11A1 |
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