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:0080322 | polycystic kidney disease | HGNC:14064 | Homo sapiens (human) | 10013 | HDAC6 |
|
||
| DOID:8991 | cervix uteri carcinoma in situ | HGNC:14064 | Homo sapiens (human) | 10013 | HDAC6 |
|
||
| DOID:4947 | cholangiocarcinoma | HGNC:14064 | Homo sapiens (human) | 10013 | HDAC6 |
|
||
| DOID:0112106 | chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia | HGNC:14064 | Homo sapiens (human) | 10013 | HDAC6 |
|
||
| DOID:9970 | obesity | HGNC:14063 | Homo sapiens (human) | 9759 | HDAC4 |
|
||
| DOID:1875 | impotence | HGNC:14063 | Homo sapiens (human) | 9759 | HDAC4 |
|
||
| DOID:684 | hepatocellular carcinoma | HGNC:14063 | Homo sapiens (human) | 9759 | HDAC4 |
|
||
| DOID:332 | amyotrophic lateral sclerosis | HGNC:14063 | Homo sapiens (human) | 9759 | HDAC4 |
|
||
| DOID:8670 | eating disorder | HGNC:14063 | Homo sapiens (human) | 9759 | HDAC4 |
|
||
| DOID:3525 | middle cerebral artery infarction | HGNC:14063 | Homo sapiens (human) | 9759 | HDAC4 |
|
||
| DOID:3627 | aortic aneurysm | HGNC:14063 | Homo sapiens (human) | 9759 | HDAC4 |
|
||
| DOID:12704 | ataxia telangiectasia | HGNC:14063 | Homo sapiens (human) | 9759 | HDAC4 |
|
||
| DOID:0050696 | fetal alcohol spectrum disorder | HGNC:14063 | Homo sapiens (human) | 9759 | HDAC4 |
|
||
| DOID:8466 | retinal degeneration | HGNC:14063 | Homo sapiens (human) | 9759 | HDAC4 |
|
||
| DOID:6432 | pulmonary hypertension | HGNC:14063 | Homo sapiens (human) | 9759 | HDAC4 |
|
||
| DOID:9952 | acute lymphoblastic leukemia | HGNC:14063 | Homo sapiens (human) | 9759 | HDAC4 |
|
||
| DOID:1825 | childhood absence epilepsy | HGNC:1406 | Homo sapiens (human) | 10369 | CACNG2 |
|
||
| DOID:0070040 | autosomal dominant intellectual developmental disorder 10 | HGNC:1406 | Homo sapiens (human) | 10369 | CACNG2 |
|
||
| DOID:8545 | malignant hyperthermia | HGNC:1405 | Homo sapiens (human) | 786 | CACNG1 |
|
||
| DOID:5419 | schizophrenia | HGNC:14026 | Homo sapiens (human) | 64478 | CSMD1 |
|
||
| DOID:1596 | depressive disorder | HGNC:14025 | Homo sapiens (human) | 60482 | SLC5A7 |
|
||
| DOID:0110661 | congenital myasthenic syndrome 20 | HGNC:14025 | Homo sapiens (human) | 60482 | SLC5A7 |
|
||
| DOID:0111199 | autosomal dominant distal hereditary motor neuronopathy 7 | HGNC:14025 | Homo sapiens (human) | 60482 | SLC5A7 |
|
||
| DOID:2841 | asthma | HGNC:14025 | Homo sapiens (human) | 60482 | SLC5A7 |
|
||
| DOID:1470 | major depressive disorder | HGNC:14025 | Homo sapiens (human) | 60482 | SLC5A7 |
|
