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:0070398 | hypomyelinating leukodystrophy 15 | MGI:97838 | Mus musculus (house mouse) | 107508 | Eprs1 |
|
||
| DOID:3389 | Papillon-Lefevre disease | HGNC:2528 | Homo sapiens (human) | 1075 | CTSC |
|
||
| DOID:9970 | obesity | HGNC:2528 | Homo sapiens (human) | 1075 | CTSC |
|
||
| DOID:2316 | brain ischemia | HGNC:2528 | Homo sapiens (human) | 1075 | CTSC |
|
||
| DOID:1474 | aggressive periodontitis | HGNC:2528 | Homo sapiens (human) | 1075 | CTSC |
|
||
| DOID:5419 | schizophrenia | HGNC:2528 | Homo sapiens (human) | 1075 | CTSC |
|
||
| DOID:10763 | hypertension | HGNC:2528 | Homo sapiens (human) | 1075 | CTSC |
|
||
| DOID:0050941 | spastic ataxia 2 | HGNC:6317 | Homo sapiens (human) | 10749 | KIF1C |
|
||
| DOID:863 | nervous system disease | HGNC:6317 | Homo sapiens (human) | 10749 | KIF1C |
|
||
| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | MGI:108451 | Mus musculus (house mouse) | 107476 | Acaca |
|
||
| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | MGI:108451 | Mus musculus (house mouse) | 107476 | Acaca |
|
||
| DOID:0060404 | chromosome 17q12 deletion syndrome | MGI:108451 | Mus musculus (house mouse) | 107476 | Acaca |
|
||
| DOID:9452 | steatotic liver disease | MGI:108451 | Mus musculus (house mouse) | 107476 | Acaca |
|
||
| DOID:0080000 | muscular disease | MGI:108451 | Mus musculus (house mouse) | 107476 | Acaca |
|
||
| DOID:0060853 | Potocki-Lupski syndrome | HGNC:9834 | Homo sapiens (human) | 10743 | RAI1 |
|
||
| DOID:0060768 | Smith-Magenis syndrome | HGNC:9834 | Homo sapiens (human) | 10743 | RAI1 |
|
||
| DOID:0080865 | primary ovarian insufficiency 8 | HGNC:11356 | Homo sapiens (human) | 10734 | STAG3 |
|
||
| DOID:0112350 | spermatogenic failure 61 | HGNC:11356 | Homo sapiens (human) | 10734 | STAG3 |
|
||
| DOID:0110202 | Charcot-Marie-Tooth disease dominant intermediate A | MGI:1861607 | Mus musculus (house mouse) | 107338 | Gbf1 |
|
||
| DOID:700 | mitochondrial metabolism disease | HGNC:12843 | Homo sapiens (human) | 10730 | YME1L1 |
|
||
| DOID:12930 | dilated cardiomyopathy | HGNC:12843 | Homo sapiens (human) | 10730 | YME1L1 |
|
||
| DOID:0111436 | optic atrophy 11 | HGNC:12843 | Homo sapiens (human) | 10730 | YME1L1 |
|
||
| DOID:0050861 | colorectal adenocarcinoma | HGNC:12843 | Homo sapiens (human) | 10730 | YME1L1 |
|
||
| DOID:1936 | atherosclerosis | HGNC:16049 | Homo sapiens (human) | 10728 | PTGES3 |
|
||
| DOID:3181 | oligodendroglioma | HGNC:16049 | Homo sapiens (human) | 10728 | PTGES3 |
|
