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:12858 | Huntington's disease | SGD:S000005560 | Saccharomyces cerevisiae S288C | 854199 | AKR2 |
|
||
| DOID:557 | kidney disease | HGNC:618 | Homo sapiens (human) | 8542 | APOL1 |
|
||
| DOID:0111446 | progressive myoclonus epilepsy 3 | SGD:S000005569 | Saccharomyces cerevisiae S288C | 854208 | WHI2 |
|
||
| DOID:0080560 | congenital disorder of glycosylation Ih | SGD:S000005593 | Saccharomyces cerevisiae S288C | 854233 | ALG8 |
|
||
| DOID:0050570 | congenital disorder of glycosylation type I | SGD:S000005593 | Saccharomyces cerevisiae S288C | 854233 | ALG8 |
|
||
| DOID:0080319 | X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia | SGD:S000005611 | Saccharomyces cerevisiae S288C | 854252 | OST3 |
|
||
| DOID:0081183 | autosomal recessive intellectual developmental disorder 7 | SGD:S000005611 | Saccharomyces cerevisiae S288C | 854252 | OST3 |
|
||
| DOID:612 | primary immunodeficiency disease | SGD:S000005611 | Saccharomyces cerevisiae S288C | 854252 | OST3 |
|
||
| DOID:10283 | prostate cancer | SGD:S000005611 | Saccharomyces cerevisiae S288C | 854252 | OST3 |
|
||
| DOID:104 | bacterial infectious disease | SGD:S000005611 | Saccharomyces cerevisiae S288C | 854252 | OST3 |
|
||
| DOID:0111839 | congenital disorder of glycosylation Icc | SGD:S000005611 | Saccharomyces cerevisiae S288C | 854252 | OST3 |
|
||
| DOID:1596 | depressive disorder | RGD:69270 | Rattus norvegicus (Norway rat) | 85426 | Slc5a7 |
|
||
| DOID:0110661 | congenital myasthenic syndrome 20 | RGD:69270 | Rattus norvegicus (Norway rat) | 85426 | Slc5a7 |
|
||
| DOID:2841 | asthma | RGD:69270 | Rattus norvegicus (Norway rat) | 85426 | Slc5a7 |
|
||
| DOID:1470 | major depressive disorder | RGD:69270 | Rattus norvegicus (Norway rat) | 85426 | Slc5a7 |
|
||
| DOID:0111199 | autosomal dominant distal hereditary motor neuronopathy 7 | RGD:69270 | Rattus norvegicus (Norway rat) | 85426 | Slc5a7 |
|
||
| DOID:0060307 | autosomal dominant intellectual developmental disorder | SGD:S000005619 | Saccharomyces cerevisiae S288C | 854260 | CMR2 |
|
||
| DOID:14330 | Parkinson's disease | SGD:S000005635 | Saccharomyces cerevisiae S288C | 854276 | INP53 |
|
||
| DOID:0080464 | developmental and epileptic encephalopathy 53 | SGD:S000005635 | Saccharomyces cerevisiae S288C | 854276 | INP53 |
|
||
| DOID:0060898 | Parkinson's disease 20 | SGD:S000005635 | Saccharomyces cerevisiae S288C | 854276 | INP53 |
|
||
| DOID:14250 | Down syndrome | SGD:S000005635 | Saccharomyces cerevisiae S288C | 854276 | INP53 |
|
||
| DOID:0060894 | early-onset Parkinson's disease | SGD:S000005635 | Saccharomyces cerevisiae S288C | 854276 | INP53 |
|
||
| DOID:0111155 | autosomal recessive spinocerebellar ataxia 21 | SGD:S000005638 | Saccharomyces cerevisiae S288C | 854279 | CEX1 |
|
||
| DOID:0050951 | hereditary ataxia | SGD:S000005638 | Saccharomyces cerevisiae S288C | 854279 | CEX1 |
|
||
| DOID:0111069 | congenital bile acid synthesis defect 2 | SGD:S000005646 | Saccharomyces cerevisiae S288C | 854287 | GCY1 |
|
