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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:0111399 | congenital dyserythropoietic anemia type III | HGNC:6392 | Homo sapiens (human) | 9493 | KIF23 |
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| DOID:0111392 | mucopolysaccharidosis type IVB | HGNC:4298 | Homo sapiens (human) | 2720 | GLB1 |
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| DOID:0112136 | severe congenital neutropenia 4 | HGNC:24861 | Homo sapiens (human) | 92579 | G6PC3 |
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| DOID:0111997 | immunodeficiency 63 | HGNC:6009 | Homo sapiens (human) | 3560 | IL2RB |
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| DOID:4751 | striatonigral degeneration | HGNC:8066 | Homo sapiens (human) | 23636 | NUP62 |
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| DOID:0112358 | short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies | HGNC:13655 | Homo sapiens (human) | 222663 | SCUBE3 |
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| DOID:0080326 | familial hypertrophic cardiomyopathy | HGNC:17574 | Homo sapiens (human) | 57538 | ALPK3 |
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| DOID:0081288 | white sponge nevus 2 | HGNC:6415 | Homo sapiens (human) | 3860 | KRT13 |
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| DOID:0050814 | temtamy preaxial brachydactyly syndrome | HGNC:17198 | Homo sapiens (human) | 22856 | CHSY1 |
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| DOID:11713 | diabetic angiopathy | HGNC:11180 | Homo sapiens (human) | 6648 | SOD2 |
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| DOID:0080441 | developmental and epileptic encephalopathy 49 | HGNC:19344 | Homo sapiens (human) | 23258 | DENND5A |
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| DOID:648 | kuru | HGNC:9449 | Homo sapiens (human) | 5621 | PRNP |
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| DOID:0111308 | familial febrile seizures 11 | HGNC:17245 | Homo sapiens (human) | 57094 | CPA6 |
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| DOID:0050777 | Joubert syndrome | HGNC:694 | Homo sapiens (human) | 403 | ARL3 |
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| DOID:13533 | osteopetrosis | HGNC:11028 | Homo sapiens (human) | 6522 | SLC4A2 |
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| DOID:0070271 | Lynch syndrome 1 | HGNC:7325 | Homo sapiens (human) | 4436 | MSH2 |
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| DOID:0111678 | hereditary folate malabsorption | HGNC:30521 | Homo sapiens (human) | 113235 | SLC46A1 |
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| DOID:0050591 | tooth agenesis | HGNC:6698 | Homo sapiens (human) | 4040 | LRP6 |
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| DOID:0111238 | congenital muscular dystrophy-dystroglycanopathy type A13 | HGNC:15685 | Homo sapiens (human) | 11041 | B4GAT1 |
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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:0070210 | hereditary lymphedema IA | HGNC:3767 | Homo sapiens (human) | 2324 | FLT4 |
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| DOID:0111098 | Fanconi anemia complementation group B | HGNC:3583 | Homo sapiens (human) | 2187 | FANCB |
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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:0110965 | brachydactyly type A2 | HGNC:1069 | Homo sapiens (human) | 650 | BMP2 |
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