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:0050328 | congenital hypothyroidism | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
|
||
| DOID:0060180 | colitis | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
|
||
| DOID:3891 | placental insufficiency | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
|
||
| DOID:1907 | malignant fibrous histiocytoma | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
|
||
| DOID:7998 | hyperthyroidism | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
|
||
| DOID:332 | amyotrophic lateral sclerosis | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
|
||
| DOID:0050700 | cardiomyopathy | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
|
||
| DOID:0060611 | abdominal obesity-metabolic syndrome | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
|
||
| DOID:12858 | Huntington's disease | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
|
||
| DOID:12236 | primary biliary cholangitis | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
|
||
| DOID:263 | kidney cancer | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
|
||
| DOID:10871 | age related macular degeneration | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
|
||
| DOID:1074 | kidney failure | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
|
||
| DOID:114 | heart disease | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
|
||
| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
|
||
| DOID:11716 | prediabetes syndrome | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
|
||
| DOID:10376 | amblyopia | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
|
||
| DOID:14330 | Parkinson's disease | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
|
||
| DOID:9352 | type 2 diabetes mellitus | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
|
||
| DOID:3083 | chronic obstructive pulmonary disease | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
|
||
| DOID:12930 | dilated cardiomyopathy | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
|
||
| DOID:5844 | myocardial infarction | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
|
||
| DOID:4448 | macular degeneration | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
|
||
| DOID:4195 | hyperglycemia | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
|
||
| DOID:8947 | diabetic retinopathy | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
|
