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:5419 | schizophrenia | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
|
||
| DOID:3073 | brain glioblastoma multiforme | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
|
||
| DOID:4947 | cholangiocarcinoma | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
|
||
| DOID:3312 | bipolar disorder | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
|
||
| DOID:0060318 | acute promyelocytic leukemia | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
|
||
| DOID:657 | adenoma | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
|
||
| DOID:0050700 | cardiomyopathy | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
|
||
| DOID:1459 | hypothyroidism | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
|
||
| DOID:6000 | congestive heart failure | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
|
||
| DOID:2560 | morphine dependence | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
|
||
| DOID:1574 | alcohol use disorder | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
|
||
| DOID:0050742 | nicotine dependence | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
|
||
| DOID:5844 | myocardial infarction | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
|
||
| DOID:1793 | pancreatic cancer | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
|
||
| DOID:0050933 | ovarian serous carcinoma | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
|
||
| DOID:10652 | Alzheimer's disease | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
|
||
| DOID:0110734 | neurodegeneration with brain iron accumulation | HGNC:7694 | Homo sapiens (human) | 4706 | NDUFAB1 |
|
||
| DOID:0080488 | mucolipidosis | HGNC:7758 | Homo sapiens (human) | 4758 | NEU1 |
|
||
| DOID:3343 | glycoproteinosis | HGNC:7758 | Homo sapiens (human) | 4758 | NEU1 |
|
||
| DOID:863 | nervous system disease | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
|
||
| DOID:1574 | alcohol use disorder | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
|
||
| DOID:0050635 | alternating hemiplegia of childhood | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
|
||
| DOID:0111182 | familial hemiplegic migraine 2 | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
|
||
| DOID:10024 | migraine with aura | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
|
||
| DOID:0070384 | developmental and epileptic encephalopathy 98 | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
|
