Table Filtering
Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID ▼ | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:1574 | alcohol use disorder | HGNC:23064 | Homo sapiens (human) | 119391 | GSTO2 |
|
||
| DOID:2841 | asthma | HGNC:23064 | Homo sapiens (human) | 119391 | GSTO2 |
|
||
| DOID:10584 | retinitis pigmentosa | HGNC:23059 | Homo sapiens (human) | 63827 | BCAN |
|
||
| DOID:3525 | middle cerebral artery infarction | HGNC:23059 | Homo sapiens (human) | 63827 | BCAN |
|
||
| DOID:3070 | high grade glioma | HGNC:23059 | Homo sapiens (human) | 63827 | BCAN |
|
||
| DOID:5212 | congenital disorder of glycosylation | HGNC:23056 | Homo sapiens (human) | 10195 | ALG3 |
|
||
| DOID:0080556 | congenital disorder of glycosylation Id | HGNC:23056 | Homo sapiens (human) | 10195 | ALG3 |
|
||
| DOID:3343 | glycoproteinosis | HGNC:23026 | Homo sapiens (human) | 84572 | GNPTG |
|
||
| DOID:0080678 | mucolipidosis III gamma | HGNC:23026 | Homo sapiens (human) | 84572 | GNPTG |
|
||
| DOID:0060174 | GABA aminotransferase deficiency | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
|
||
| DOID:10763 | hypertension | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
|
||
| DOID:9976 | heroin dependence | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
|
||
| DOID:11832 | visual epilepsy | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
|
||
| DOID:0080855 | Parkinsonism | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
|
||
| DOID:10652 | Alzheimer's disease | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
|
||
| DOID:2548 | reflex epilepsy | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
|
||
| DOID:0050562 | West syndrome | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
|
||
| DOID:12858 | Huntington's disease | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
|
||
| DOID:1824 | status epilepticus | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
|
||
| DOID:1596 | depressive disorder | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
|
||
| DOID:326 | ischemia | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
|
||
| DOID:0060256 | Dowling-Degos disease | HGNC:22954 | Homo sapiens (human) | 56983 | POGLUT1 |
|
||
| DOID:0080762 | autosomal recessive limb-girdle muscular dystrophy type 2Z | HGNC:22954 | Homo sapiens (human) | 56983 | POGLUT1 |
|
||
| DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | HGNC:22954 | Homo sapiens (human) | 56983 | POGLUT1 |
|
||
| DOID:0112374 | muscular dystrophy-dystroglycanopathy | HGNC:22932 | Homo sapiens (human) | 29925 | GMPPB |
|
