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:0080108 | myoglobinuria | HGNC:8889 | Homo sapiens (human) | 5224 | PGAM2 |
|
||
| DOID:0112275 | developmental and epileptic encephalopathy 93 | HGNC:851 | Homo sapiens (human) | 523 | ATP6V1A |
|
||
| DOID:0070129 | autosomal recessive cutis laxa type IID | HGNC:851 | Homo sapiens (human) | 523 | ATP6V1A |
|
||
| DOID:0111933 | phosphoglycerate kinase 1 deficiency | HGNC:8896 | Homo sapiens (human) | 5230 | PGK1 |
|
||
| DOID:162 | cancer | HGNC:8896 | Homo sapiens (human) | 5230 | PGK1 |
|
||
| DOID:583 | hemolytic anemia | HGNC:8896 | Homo sapiens (human) | 5230 | PGK1 |
|
||
| DOID:14330 | Parkinson's disease | HGNC:8896 | Homo sapiens (human) | 5230 | PGK1 |
|
||
| DOID:14330 | Parkinson's disease | HGNC:8898 | Homo sapiens (human) | 5232 | PGK2 |
|
||
| DOID:162 | cancer | HGNC:8898 | Homo sapiens (human) | 5232 | PGK2 |
|
||
| DOID:1380 | endometrial cancer | HGNC:8905 | Homo sapiens (human) | 5236 | PGM1 |
|
||
| DOID:3307 | teratoma | HGNC:8905 | Homo sapiens (human) | 5236 | PGM1 |
|
||
| DOID:0080570 | congenital disorder of glycosylation It | HGNC:8905 | Homo sapiens (human) | 5236 | PGM1 |
|
||
| DOID:4362 | cervical cancer | HGNC:8907 | Homo sapiens (human) | 5238 | PGM3 |
|
||
| DOID:3307 | teratoma | HGNC:8907 | Homo sapiens (human) | 5238 | PGM3 |
|
||
| DOID:0111953 | immunodeficiency 23 | HGNC:8907 | Homo sapiens (human) | 5238 | PGM3 |
|
||
| DOID:162 | cancer | HGNC:8907 | Homo sapiens (human) | 5238 | PGM3 |
|
||
| DOID:2747 | glycogen storage disease | HGNC:8925 | Homo sapiens (human) | 5255 | PHKA1 |
|
||
| DOID:1459 | hypothyroidism | HGNC:8925 | Homo sapiens (human) | 5255 | PHKA1 |
|
||
| DOID:0111040 | glycogen storage disease IXd | HGNC:8925 | Homo sapiens (human) | 5255 | PHKA1 |
|
||
| DOID:0050545 | visceral heterotaxy | HGNC:8926 | Homo sapiens (human) | 5256 | PHKA2 |
|
||
| DOID:0111042 | glycogen storage disease IXa | HGNC:8926 | Homo sapiens (human) | 5256 | PHKA2 |
|
||
| DOID:2747 | glycogen storage disease | HGNC:8926 | Homo sapiens (human) | 5256 | PHKA2 |
|
||
| DOID:0111041 | glycogen storage disease IXb | HGNC:8927 | Homo sapiens (human) | 5257 | PHKB |
|
||
| DOID:5082 | liver cirrhosis | HGNC:8931 | Homo sapiens (human) | 5261 | PHKG2 |
|
||
| DOID:2747 | glycogen storage disease | HGNC:8931 | Homo sapiens (human) | 5261 | PHKG2 |
|
