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:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:14934 | Homo sapiens (human) | 51548 | SIRT6 |
|
||
| DOID:224 | transient cerebral ischemia | HGNC:14934 | Homo sapiens (human) | 51548 | SIRT6 |
|
||
| DOID:3911 | progeria | HGNC:14934 | Homo sapiens (human) | 51548 | SIRT6 |
|
||
| DOID:9970 | obesity | HGNC:14934 | Homo sapiens (human) | 51548 | SIRT6 |
|
||
| DOID:0014667 | disease of metabolism | HGNC:8806 | Homo sapiens (human) | 5160 | PDHA1 |
|
||
| DOID:3649 | pyruvate decarboxylase deficiency | HGNC:8806 | Homo sapiens (human) | 5160 | PDHA1 |
|
||
| DOID:8466 | retinal degeneration | HGNC:8806 | Homo sapiens (human) | 5160 | PDHA1 |
|
||
| DOID:0080140 | multiple congenital anomalies-hypotonia-seizures syndrome 3 | HGNC:14938 | Homo sapiens (human) | 51604 | PIGT |
|
||
| DOID:0060284 | paroxysmal nocturnal hemoglobinuria | HGNC:14938 | Homo sapiens (human) | 51604 | PIGT |
|
||
| DOID:0014667 | disease of metabolism | HGNC:8807 | Homo sapiens (human) | 5161 | PDHA2 |
|
||
| DOID:3649 | pyruvate decarboxylase deficiency | HGNC:8807 | Homo sapiens (human) | 5161 | PDHA2 |
|
||
| DOID:0111910 | spermatogenic failure | HGNC:8807 | Homo sapiens (human) | 5161 | PDHA2 |
|
||
| DOID:8466 | retinal degeneration | HGNC:8807 | Homo sapiens (human) | 5161 | PDHA2 |
|
||
| DOID:3649 | pyruvate decarboxylase deficiency | HGNC:8808 | Homo sapiens (human) | 5162 | PDHB |
|
||
| DOID:9352 | type 2 diabetes mellitus | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
|
||
| DOID:783 | end stage renal disease | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
|
||
| DOID:3068 | glioblastoma | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
|
||
| DOID:2738 | pseudoxanthoma elasticum | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
|
||
| DOID:0080333 | aortic valve disease 1 | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
|
||
| DOID:1123 | spondyloarthropathy | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
|
||
| DOID:1287 | cardiovascular system disease | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
|
||
| DOID:8398 | osteoarthritis | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
|
||
| DOID:9970 | obesity | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
|
||
| DOID:0060887 | ossification of the posterior longitudinal ligament of spine | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
|
||
| DOID:0050644 | arterial calcification of infancy | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
|
