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:1686 | glaucoma | HGNC:13557 | Homo sapiens (human) | 59272 | ACE2 |
|
||
| DOID:850 | lung disease | HGNC:13557 | Homo sapiens (human) | 59272 | ACE2 |
|
||
| DOID:10763 | hypertension | HGNC:13557 | Homo sapiens (human) | 59272 | ACE2 |
|
||
| DOID:3525 | middle cerebral artery infarction | HGNC:13557 | Homo sapiens (human) | 59272 | ACE2 |
|
||
| DOID:0070221 | progressive familial intrahepatic cholestasis | HGNC:13543 | Homo sapiens (human) | 23120 | ATP10B |
|
||
| DOID:0111239 | congenital muscular dystrophy-dystroglycanopathy type A10 | HGNC:13530 | Homo sapiens (human) | 10329 | RXYLT1 |
|
||
| DOID:0050560 | Walker-Warburg syndrome | HGNC:13530 | Homo sapiens (human) | 10329 | RXYLT1 |
|
||
| DOID:0060302 | type II complement component 8 deficiency | HGNC:1353 | Homo sapiens (human) | 732 | C8B |
|
||
| DOID:5844 | myocardial infarction | HGNC:1353 | Homo sapiens (human) | 732 | C8B |
|
||
| DOID:0050598 | extrapulmonary tuberculosis | HGNC:13523 | Homo sapiens (human) | 10332 | CLEC4M |
|
||
| DOID:2957 | pulmonary tuberculosis | HGNC:13523 | Homo sapiens (human) | 10332 | CLEC4M |
|
||
| DOID:2945 | severe acute respiratory syndrome | HGNC:13523 | Homo sapiens (human) | 10332 | CLEC4M |
|
||
| DOID:0111849 | osteogenesis imperfecta type 20 | HGNC:13520 | Homo sapiens (human) | 23184 | MESD |
|
||
| DOID:5844 | myocardial infarction | HGNC:1352 | Homo sapiens (human) | 731 | C8A |
|
||
| DOID:0060301 | type I complement component 8 deficiency | HGNC:1352 | Homo sapiens (human) | 731 | C8A |
|
||
| DOID:1441 | autosomal dominant cerebellar ataxia | HGNC:1349 | Homo sapiens (human) | 219285 | SAMD9L |
|
||
| DOID:0050908 | myelodysplastic syndrome | HGNC:1349 | Homo sapiens (human) | 219285 | SAMD9L |
|
||
| DOID:1094 | attention deficit hyperactivity disorder | HGNC:13488 | Homo sapiens (human) | 27183 | VPS4A |
|
||
| DOID:936 | brain disease | HGNC:13481 | Homo sapiens (human) | 81622 | UNC93B1 |
|
||
| DOID:0080170 | normophosphatemic familial tumoral calcinosis | HGNC:1348 | Homo sapiens (human) | 54809 | SAMD9 |
|
||
| DOID:0060300 | complement component 7 deficiency | HGNC:1346 | Homo sapiens (human) | 730 | C7 |
|
||
| DOID:10976 | membranous glomerulonephritis | HGNC:1346 | Homo sapiens (human) | 730 | C7 |
|
||
| DOID:5844 | myocardial infarction | HGNC:1346 | Homo sapiens (human) | 730 | C7 |
|
||
| DOID:11832 | visual epilepsy | HGNC:1346 | Homo sapiens (human) | 730 | C7 |
|
||
| DOID:0060929 | non-syndromic X-linked intellectual developmental disorder 111 | HGNC:13449 | Homo sapiens (human) | 84631 | SLITRK2 |
|
