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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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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:326 | ischemia | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:3744 | cervical squamous cell carcinoma | HGNC:959 | Homo sapiens (human) | 581 | BAX |
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| DOID:0110640 | congenital muscular dystrophy due to LMNA mutation | HGNC:6637 | Homo sapiens (human) | 4001 | LMNB1 |
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| DOID:2908 | Treacher Collins syndrome | HGNC:11654 | Homo sapiens (human) | 6949 | TCOF1 |
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| DOID:0060350 | adenine phosphoribosyltransferase deficiency | HGNC:626 | Homo sapiens (human) | 353 | APRT |
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| DOID:11446 | sciatic neuropathy | HGNC:6783 | Homo sapiens (human) | 4099 | MAG |
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| DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | HGNC:17649 | Homo sapiens (human) | 64208 | POPDC3 |
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| DOID:1470 | major depressive disorder | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:1070 | primary open angle glaucoma | HGNC:6487 | Homo sapiens (human) | 3913 | LAMB2 |
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| DOID:0110539 | autosomal recessive nonsyndromic deafness 97 | HGNC:7029 | Homo sapiens (human) | 4233 | MET |
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| DOID:1485 | cystic fibrosis | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:8947 | diabetic retinopathy | HGNC:2500 | Homo sapiens (human) | 1490 | CCN2 |
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| DOID:3492 | mixed connective tissue disease | HGNC:11153 | Homo sapiens (human) | 6628 | SNRPB |
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| DOID:12143 | neurogenic bladder | HGNC:7808 | Homo sapiens (human) | 4803 | NGF |
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| DOID:2377 | multiple sclerosis | HGNC:320 | Homo sapiens (human) | 177 | AGER |
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| DOID:219 | colon cancer | HGNC:11905 | Homo sapiens (human) | 8795 | TNFRSF10B |
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| DOID:11832 | visual epilepsy | HGNC:29595 | Homo sapiens (human) | 130120 | REG3G |
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| DOID:9976 | heroin dependence | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:11830 | myopia | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:0050700 | cardiomyopathy | HGNC:9314 | Homo sapiens (human) | 5530 | PPP3CA |
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| DOID:3312 | bipolar disorder | HGNC:1102 | Homo sapiens (human) | 23774 | BRD1 |
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| DOID:4607 | biliary tract cancer | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:0050169 | cutaneous lupus erythematosus | HGNC:11935 | Homo sapiens (human) | 959 | CD40LG |
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| DOID:2355 | anemia | HGNC:492 | Homo sapiens (human) | 286 | ANK1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:8004 | Homo sapiens (human) | 8829 | NRP1 |
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