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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol ▼ | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0050692 | Brody myopathy | HGNC:813 | Homo sapiens (human) | 489 | ATP2A3 |
|
||
| DOID:10763 | hypertension | HGNC:813 | Homo sapiens (human) | 489 | ATP2A3 |
|
||
| DOID:1826 | epilepsy | HGNC:806 | Homo sapiens (human) | 483 | ATP1B3 |
|
||
| DOID:1826 | epilepsy | HGNC:805 | Homo sapiens (human) | 482 | ATP1B2 |
|
||
| DOID:1826 | epilepsy | HGNC:804 | Homo sapiens (human) | 481 | ATP1B1 |
|
||
| DOID:10003 | sensorineural hearing loss | HGNC:804 | Homo sapiens (human) | 481 | ATP1B1 |
|
||
| DOID:10825 | essential hypertension | HGNC:804 | Homo sapiens (human) | 481 | ATP1B1 |
|
||
| DOID:0070384 | developmental and epileptic encephalopathy 98 | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
|
||
| DOID:0060178 | familial hemiplegic migraine | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
|
||
| DOID:9279 | hyperhomocysteinemia | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
|
||
| DOID:10763 | hypertension | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
|
||
| DOID:1574 | alcohol use disorder | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
|
||
| DOID:10024 | migraine with aura | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
|
||
| DOID:863 | nervous system disease | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
|
||
| DOID:14264 | benign neonatal seizures | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
|
||
| DOID:0111182 | familial hemiplegic migraine 2 | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
|
||
| DOID:0111558 | Charcot-Marie-Tooth disease type 2DD | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
|
||
| DOID:1826 | epilepsy | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
|
||
| DOID:0050635 | alternating hemiplegia of childhood | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
|
||
| DOID:863 | nervous system disease | HGNC:799 | Homo sapiens (human) | 476 | ATP1A1 |
|
||
| DOID:9279 | hyperhomocysteinemia | HGNC:799 | Homo sapiens (human) | 476 | ATP1A1 |
|
||
| DOID:0111558 | Charcot-Marie-Tooth disease type 2DD | HGNC:799 | Homo sapiens (human) | 476 | ATP1A1 |
|
||
| DOID:0060178 | familial hemiplegic migraine | HGNC:799 | Homo sapiens (human) | 476 | ATP1A1 |
|
||
| DOID:1574 | alcohol use disorder | HGNC:799 | Homo sapiens (human) | 476 | ATP1A1 |
|
||
| DOID:10003 | sensorineural hearing loss | HGNC:799 | Homo sapiens (human) | 476 | ATP1A1 |
|
