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:0111271 | Oliver-McFarlane syndrome | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
|
||
| DOID:0112219 | developmental and epileptic encephalopathy 84 | HGNC:12525 | Homo sapiens (human) | 7358 | UGDH |
|
||
| DOID:0050770 | polycystic liver disease | HGNC:4138 | Homo sapiens (human) | 23193 | GANAB |
|
||
| DOID:9976 | heroin dependence | HGNC:4092 | Homo sapiens (human) | 2571 | GAD1 |
|
||
| DOID:0080351 | CLOVES syndrome | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
|
||
| DOID:9976 | heroin dependence | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
|
||
| DOID:0050144 | Kartagener syndrome | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
|
||
| DOID:1380 | endometrial cancer | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
|
||
| DOID:648 | kuru | HGNC:9449 | Homo sapiens (human) | 5621 | PRNP |
|
||
| DOID:0110296 | autosomal recessive limb-girdle muscular dystrophy type 2M | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
|
||
| DOID:2987 | familial mediterranean fever | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
|
||
| DOID:2978 | carbohydrate metabolic disorder | HGNC:7216 | Homo sapiens (human) | 4351 | MPI |
|
||
| DOID:0050699 | Dent disease | HGNC:8108 | Homo sapiens (human) | 4952 | OCRL |
|
||
| DOID:0112275 | developmental and epileptic encephalopathy 93 | HGNC:851 | Homo sapiens (human) | 523 | ATP6V1A |
|
||
| DOID:2987 | familial mediterranean fever | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
|
||
| DOID:9269 | maple syrup urine disease | HGNC:986 | Homo sapiens (human) | 593 | BCKDHA |
|
||
| DOID:2018 | hyperinsulinism | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
|
||
| DOID:11758 | iron deficiency anemia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
|
||
| DOID:1612 | breast cancer | HGNC:587 | Homo sapiens (human) | 328 | APEX1 |
|
||
| DOID:9352 | type 2 diabetes mellitus | HGNC:381 | Homo sapiens (human) | 231 | AKR1B1 |
|
||
| DOID:0111108 | maturity-onset diabetes of the young type 10 | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
|
||
| DOID:0081223 | glycosylphosphatidylinositol biosynthesis defect 16 | HGNC:8960 | Homo sapiens (human) | 5279 | PIGC |
|
||
| DOID:2986 | IgA glomerulonephritis | HGNC:11847 | Homo sapiens (human) | 7096 | TLR1 |
|
||
| DOID:2030 | anxiety disorder | HGNC:21072 | Homo sapiens (human) | 79694 | MANEA |
|
||
| DOID:0111394 | mucopolysaccharidosis type IIIB | HGNC:7632 | Homo sapiens (human) | 4669 | NAGLU |
|
