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:1824 | status epilepticus | HGNC:612 | Homo sapiens (human) | 347 | APOD |
|
||
| DOID:4762 | vasculogenic impotence | HGNC:612 | Homo sapiens (human) | 347 | APOD |
|
||
| DOID:9970 | obesity | HGNC:612 | Homo sapiens (human) | 347 | APOD |
|
||
| DOID:9352 | type 2 diabetes mellitus | HGNC:612 | Homo sapiens (human) | 347 | APOD |
|
||
| DOID:10914 | amnestic disorder | HGNC:6126 | Homo sapiens (human) | 8660 | IRS2 |
|
||
| DOID:4194 | glucose metabolism disease | HGNC:6126 | Homo sapiens (human) | 8660 | IRS2 |
|
||
| DOID:1059 | intellectual disability | HGNC:6126 | Homo sapiens (human) | 8660 | IRS2 |
|
||
| DOID:11476 | osteoporosis | HGNC:6126 | Homo sapiens (human) | 8660 | IRS2 |
|
||
| DOID:9352 | type 2 diabetes mellitus | HGNC:6126 | Homo sapiens (human) | 8660 | IRS2 |
|
||
| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:6126 | Homo sapiens (human) | 8660 | IRS2 |
|
||
| DOID:10652 | Alzheimer's disease | HGNC:6126 | Homo sapiens (human) | 8660 | IRS2 |
|
||
| DOID:0080572 | congenital disorder of glycosylation Iw | HGNC:6172 | Homo sapiens (human) | 3703 | STT3A |
|
||
| DOID:9351 | diabetes mellitus | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
|
||
| DOID:0070218 | familial hyperinsulinemic hypoglycemia 2 | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
|
||
| DOID:9352 | type 2 diabetes mellitus | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
|
||
| DOID:10763 | hypertension | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
|
||
| DOID:0060639 | permanent neonatal diabetes mellitus | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
|
||
| DOID:11716 | prediabetes syndrome | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
|
||
| DOID:11446 | sciatic neuropathy | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
|
||
| DOID:11832 | visual epilepsy | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
|
||
| DOID:2018 | hyperinsulinism | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
|
||
| DOID:1824 | status epilepticus | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
|
||
| DOID:0080855 | Parkinsonism | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
|
||
| DOID:0111110 | maturity-onset diabetes of the young type 13 | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
|
||
| DOID:684 | hepatocellular carcinoma | HGNC:626 | Homo sapiens (human) | 353 | APRT |
|
