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:0112105 | X-linked parkinsonism-spasticity syndrome | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
|
||
| DOID:0060806 | syndromic X-linked intellectual disability Hedera type | FB:FBgn0037671 | Drosophila melanogaster (fruit fly) | 41104 | ATP6AP2 |
|
||
| DOID:0060309 | syndromic X-linked intellectual disability | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
|
||
| DOID:0112105 | X-linked parkinsonism-spasticity syndrome | FB:FBgn0037671 | Drosophila melanogaster (fruit fly) | 41104 | ATP6AP2 |
|
||
| DOID:0060806 | syndromic X-linked intellectual disability Hedera type | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
|
||
| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
|
||
| DOID:5212 | congenital disorder of glycosylation | FB:FBgn0037671 | Drosophila melanogaster (fruit fly) | 41104 | ATP6AP2 |
|
||
| DOID:0060309 | syndromic X-linked intellectual disability | FB:FBgn0037671 | Drosophila melanogaster (fruit fly) | 41104 | ATP6AP2 |
|
||
| DOID:0050571 | congenital disorder of glycosylation type II | FB:FBgn0037671 | Drosophila melanogaster (fruit fly) | 41104 | ATP6AP2 |
|
||
| DOID:5212 | congenital disorder of glycosylation | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
|
||
| DOID:0112002 | immunodeficiency 47 | HGNC:868 | Homo sapiens (human) | 537 | ATP6AP1 |
|
||
| DOID:863 | nervous system disease | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
|
||
| DOID:1574 | alcohol use disorder | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
|
||
| DOID:0050635 | alternating hemiplegia of childhood | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
|
||
| DOID:0111182 | familial hemiplegic migraine 2 | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
|
||
| DOID:10024 | migraine with aura | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
|
||
| DOID:0070384 | developmental and epileptic encephalopathy 98 | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
|
||
| DOID:14264 | benign neonatal seizures | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
|
||
| DOID:0060178 | familial hemiplegic migraine | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
|
||
| DOID:1826 | epilepsy | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
|
||
| DOID:10763 | hypertension | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
|
||
| DOID:9279 | hyperhomocysteinemia | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
|
||
| DOID:4947 | cholangiocarcinoma | SGD:S000004179 | Saccharomyces cerevisiae S288C | 850886 | ATG26 |
|
||
| DOID:1793 | pancreatic cancer | SGD:S000004179 | Saccharomyces cerevisiae S288C | 850886 | ATG26 |
|
||
| DOID:2741 | bilirubin metabolic disorder | SGD:S000004179 | Saccharomyces cerevisiae S288C | 850886 | ATG26 |
|
