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:0111070 | congenital bile acid synthesis defect 3 | HGNC:2652 | Homo sapiens (human) | 9420 | CYP7B1 |
|
||
| DOID:4948 | gallbladder carcinoma | HGNC:79 | Homo sapiens (human) | 28 | ABO |
|
||
| DOID:10825 | essential hypertension | HGNC:10522 | Homo sapiens (human) | 6296 | ACSM3 |
|
||
| DOID:0112218 | developmental and epileptic encephalopathy 83 | HGNC:12527 | Homo sapiens (human) | 7360 | UGP2 |
|
||
| DOID:0111451 | progressive myoclonus epilepsy 8 | HGNC:14253 | Homo sapiens (human) | 10715 | CERS1 |
|
||
| DOID:10887 | lepromatous leprosy | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
|
||
| DOID:4450 | renal cell carcinoma | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
|
||
| DOID:3659 | sialuria | HGNC:23657 | Homo sapiens (human) | 10020 | GNE |
|
||
| DOID:0050742 | nicotine dependence | HGNC:7956 | Homo sapiens (human) | 4886 | NPY1R |
|
||
| DOID:0111390 | mucopolysaccharidosis Ih | HGNC:5391 | Homo sapiens (human) | 3425 | IDUA |
|
||
| DOID:3635 | congenital myasthenic syndrome | HGNC:10979 | Homo sapiens (human) | 6576 | SLC25A1 |
|
||
| DOID:0080564 | congenital disorder of glycosylation Il | HGNC:15672 | Homo sapiens (human) | 79796 | ALG9 |
|
||
| DOID:10283 | prostate cancer | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
|
||
| DOID:0070434 | hyperphosphatasia with impaired intellectual development syndrome 2 | HGNC:23215 | Homo sapiens (human) | 84720 | PIGO |
|
||
| DOID:0111236 | congenital muscular dystrophy-dystroglycanopathy type A3 | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
|
||
| DOID:0110676 | congenital myasthenic syndrome 13 | HGNC:2995 | Homo sapiens (human) | 1798 | DPAGT1 |
|
||
| DOID:0080140 | multiple congenital anomalies-hypotonia-seizures syndrome 3 | HGNC:14938 | Homo sapiens (human) | 51604 | PIGT |
|
||
| DOID:0112105 | X-linked parkinsonism-spasticity syndrome | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
|
||
| DOID:0111231 | congenital muscular dystrophy-dystroglycanopathy type A8 | HGNC:25902 | Homo sapiens (human) | 84892 | POMGNT2 |
|
||
| DOID:5723 | optic atrophy | HGNC:29622 | Homo sapiens (human) | 27349 | MCAT |
|
||
| DOID:9884 | muscular dystrophy | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
|
||
| DOID:670 | amphetamine abuse | HGNC:4092 | Homo sapiens (human) | 2571 | GAD1 |
|
||
| DOID:0111527 | spinal muscular atrophy with progressive myoclonic epilepsy | HGNC:735 | Homo sapiens (human) | 427 | ASAH1 |
|
||
| DOID:2559 | opiate dependence | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
|
||
| DOID:0080576 | spondyloepimetaphyseal dysplasia, Genevieve-type | HGNC:19237 | Homo sapiens (human) | 54187 | NANS |
|
