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:11725 | Cornelia de Lange syndrome | HGNC:2468 | Homo sapiens (human) | 9126 | SMC3 |
|
||
| DOID:684 | hepatocellular carcinoma | HGNC:2468 | Homo sapiens (human) | 9126 | SMC3 |
|
||
| DOID:1059 | intellectual disability | HGNC:2468 | Homo sapiens (human) | 9126 | SMC3 |
|
||
| DOID:0080507 | Cornelia de Lange syndrome 3 | HGNC:2468 | Homo sapiens (human) | 9126 | SMC3 |
|
||
| DOID:1394 | urinary schistosomiasis | HGNC:1637 | Homo sapiens (human) | 912 | CD1D |
|
||
| DOID:2957 | pulmonary tuberculosis | HGNC:1637 | Homo sapiens (human) | 912 | CD1D |
|
||
| DOID:10534 | stomach cancer | HGNC:1637 | Homo sapiens (human) | 912 | CD1D |
|
||
| DOID:12206 | dengue hemorrhagic fever | HGNC:1637 | Homo sapiens (human) | 912 | CD1D |
|
||
| DOID:0111225 | centronuclear myopathy X-linked | HGNC:7452 | Homo sapiens (human) | 9110 | MTMR4 |
|
||
| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:7452 | Homo sapiens (human) | 9110 | MTMR4 |
|
||
| DOID:767 | muscular atrophy | HGNC:7452 | Homo sapiens (human) | 9110 | MTMR4 |
|
||
| DOID:0111225 | centronuclear myopathy X-linked | HGNC:7454 | Homo sapiens (human) | 9108 | MTMR7 |
|
||
| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:7454 | Homo sapiens (human) | 9108 | MTMR7 |
|
||
| DOID:14717 | centronuclear myopathy | HGNC:7454 | Homo sapiens (human) | 9108 | MTMR7 |
|
||
| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:7453 | Homo sapiens (human) | 9107 | MTMR6 |
|
||
| DOID:14717 | centronuclear myopathy | HGNC:7453 | Homo sapiens (human) | 9107 | MTMR6 |
|
||
| DOID:0111225 | centronuclear myopathy X-linked | HGNC:7453 | Homo sapiens (human) | 9107 | MTMR6 |
|
||
| DOID:1168 | familial hyperlipidemia | HGNC:9989 | Homo sapiens (human) | 9104 | RGN |
|
||
| DOID:684 | hepatocellular carcinoma | HGNC:9989 | Homo sapiens (human) | 9104 | RGN |
|
||
| DOID:10534 | stomach cancer | HGNC:9989 | Homo sapiens (human) | 9104 | RGN |
|
||
| DOID:0112213 | multiple congenital anomalies-hypotonia-seizures syndrome 4 | HGNC:14135 | Homo sapiens (human) | 9091 | PIGQ |
|
||
| DOID:0050812 | spondyloepimetaphyseal dysplasia, Pakistani type | HGNC:8604 | Homo sapiens (human) | 9060 | PAPSS2 |
|
||
| DOID:224 | transient cerebral ischemia | HGNC:18451 | Homo sapiens (human) | 90411 | MCFD2 |
|
||
| DOID:0111843 | Paganini-Miozzo syndrome | HGNC:19133 | Homo sapiens (human) | 90161 | HS6ST2 |
|
||
| DOID:0070174 | spermatogenic failure 17 | HGNC:19218 | Homo sapiens (human) | 89869 | PLCZ1 |
|
