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:612 | primary immunodeficiency disease | FB:FBgn0032015 | Drosophila melanogaster (fruit fly) | 34137 | Ostγ | CG7830 |
|
|
| DOID:0111839 | congenital disorder of glycosylation Icc | FB:FBgn0032015 | Drosophila melanogaster (fruit fly) | 34137 | Ostγ | CG7830 |
|
|
| DOID:104 | bacterial infectious disease | FB:FBgn0032015 | Drosophila melanogaster (fruit fly) | 34137 | Ostγ | CG7830 |
|
|
| DOID:0081183 | autosomal recessive intellectual developmental disorder 7 | FB:FBgn0032015 | Drosophila melanogaster (fruit fly) | 34137 | Ostγ | CG7830 |
|
|
| DOID:0110474 | autosomal recessive nonsyndromic deafness 18B | MGI:1202064 | Mus musculus (house mouse) | 18419 | Otog |
|
||
| DOID:0110530 | autosomal recessive nonsyndromic deafness 84B | MGI:3647600 | Mus musculus (house mouse) | 628870 | Otogl |
|
||
| DOID:5419 | schizophrenia | HGNC:8574 | Homo sapiens (human) | 5048 | PAFAH1B1 |
|
||
| DOID:0060469 | Miller-Dieker lissencephaly syndrome | HGNC:8574 | Homo sapiens (human) | 5048 | PAFAH1B1 |
|
||
| DOID:684 | hepatocellular carcinoma | HGNC:8574 | Homo sapiens (human) | 5048 | PAFAH1B1 |
|
||
| DOID:0050453 | lissencephaly | HGNC:8574 | Homo sapiens (human) | 5048 | PAFAH1B1 |
|
||
| DOID:0112237 | lissencephaly 1 | HGNC:8574 | Homo sapiens (human) | 5048 | PAFAH1B1 |
|
||
| DOID:11832 | visual epilepsy | HGNC:8574 | Homo sapiens (human) | 5048 | PAFAH1B1 |
|
||
| DOID:0060058 | lymphoma | HGNC:8575 | Homo sapiens (human) | 5049 | PAFAH1B2 |
|
||
| DOID:0050812 | spondyloepimetaphyseal dysplasia, Pakistani type | HGNC:8604 | Homo sapiens (human) | 9060 | PAPSS2 |
|
||
| DOID:5154 | borna disease | HGNC:8605 | Homo sapiens (human) | 8505 | PARG |
|
||
| DOID:3454 | brain infarction | HGNC:8605 | Homo sapiens (human) | 8505 | PARG |
|
||
| DOID:0070352 | stress-induced childhood-onset neurodegeneration with variable ataxia and seizures | HGNC:8605 | Homo sapiens (human) | 8505 | PARG |
|
||
| DOID:12858 | Huntington's disease | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
|
||
| DOID:14330 | Parkinson's disease | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
|
||
| DOID:1074 | kidney failure | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
|
||
| DOID:848 | arthritis | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
|
||
| DOID:6000 | congestive heart failure | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
|
||
| DOID:5517 | stomach carcinoma | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
|
||
| DOID:224 | transient cerebral ischemia | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
|
||
| DOID:417 | autoimmune disease | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
|
