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:10763 | hypertension | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
|
||
| DOID:9976 | heroin dependence | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
|
||
| DOID:11832 | visual epilepsy | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
|
||
| DOID:0080855 | Parkinsonism | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
|
||
| DOID:10652 | Alzheimer's disease | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
|
||
| DOID:2548 | reflex epilepsy | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
|
||
| DOID:0050562 | West syndrome | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
|
||
| DOID:12858 | Huntington's disease | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
|
||
| DOID:1824 | status epilepticus | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
|
||
| DOID:1596 | depressive disorder | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
|
||
| DOID:326 | ischemia | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
|
||
| DOID:0060227 | Adams-Oliver syndrome | WB:WBGene00010386 | Caenorhabditis elegans | 179990 | H12D21.10 |
|
||
| DOID:0080470 | developmental and epileptic encephalopathy 36 | WB:WBGene00011193 | Caenorhabditis elegans | 179890 | algn-13 |
|
||
| DOID:0110676 | congenital myasthenic syndrome 13 | HGNC:2995 | Homo sapiens (human) | 1798 | DPAGT1 |
|
||
| DOID:0080562 | congenital disorder of glycosylation Ij | HGNC:2995 | Homo sapiens (human) | 1798 | DPAGT1 |
|
||
| DOID:0111258 | pentosuria | WB:WBGene00000984 | Caenorhabditis elegans | 179741 | dhs-21 |
|
||
| DOID:0110170 | Charcot-Marie-Tooth disease axonal type 2Q | WB:WBGene00014098 | Caenorhabditis elegans | 179674 | ogdh-2 |
|
||
| DOID:0111453 | 2-aminoadipic 2-oxoadipic aciduria | WB:WBGene00014098 | Caenorhabditis elegans | 179674 | ogdh-2 |
|
||
| DOID:0070253 | congenital disorder of glycosylation type IIa | WB:WBGene00001645 | Caenorhabditis elegans | 179562 | gly-20 |
|
||
| DOID:2978 | carbohydrate metabolic disorder | WB:WBGene00001645 | Caenorhabditis elegans | 179562 | gly-20 |
|
||
| DOID:0112319 | Kanzaki disease | MGI:1261422 | Mus musculus (house mouse) | 17939 | Naga |
|
||
| DOID:2367 | neuroaxonal dystrophy | MGI:1261422 | Mus musculus (house mouse) | 17939 | Naga |
|
||
| DOID:479 | angiokeratoma | MGI:1261422 | Mus musculus (house mouse) | 17939 | Naga |
|
||
| DOID:0112318 | Schindler disease type 1 | MGI:1261422 | Mus musculus (house mouse) | 17939 | Naga |
|
||
| DOID:14499 | Fabry disease | MGI:1261422 | Mus musculus (house mouse) | 17939 | Naga |
|
