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:4947 | cholangiocarcinoma | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
|
||
| DOID:0050866 | oral squamous cell carcinoma | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
|
||
| DOID:576 | proteinuria | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
|
||
| DOID:0050741 | alcohol dependence | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
|
||
| DOID:3071 | gliosarcoma | HGNC:9604 | Homo sapiens (human) | 5742 | PTGS1 |
|
||
| DOID:0050524 | maturity-onset diabetes of the young | HGNC:4923 | Homo sapiens (human) | 3099 | HK2 |
|
||
| DOID:3526 | cerebral infarction | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
|
||
| DOID:9970 | obesity | HGNC:4141 | Homo sapiens (human) | 2597 | GAPDH |
|
||
| DOID:684 | hepatocellular carcinoma | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
|
||
| DOID:9452 | steatotic liver disease | HGNC:4803 | Homo sapiens (human) | 3032 | HADHB |
|
||
| DOID:10591 | pre-eclampsia | HGNC:386 | Homo sapiens (human) | 8644 | AKR1C3 |
|
||
| DOID:0080855 | Parkinsonism | HGNC:4243 | Homo sapiens (human) | 2674 | GFRA1 |
|
||
| DOID:2349 | arteriosclerosis | HGNC:381 | Homo sapiens (human) | 231 | AKR1B1 |
|
||
| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:19358 | Homo sapiens (human) | 79087 | ALG12 |
|
||
| DOID:0111240 | congenital muscular dystrophy-dystroglycanopathy type A2 | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
|
||
| DOID:3146 | lipid metabolism disorder | HGNC:2859 | Homo sapiens (human) | 1718 | DHCR24 |
|
||
| DOID:0112147 | retinitis pigmentosa 90 | HGNC:5384 | Homo sapiens (human) | 3419 | IDH3A |
|
||
| DOID:4194 | glucose metabolism disease | HGNC:8976 | Homo sapiens (human) | 5291 | PIK3CB |
|
||
| DOID:0050585 | congenital generalized lipodystrophy | HGNC:8754 | Homo sapiens (human) | 5130 | PCYT1A |
|
||
| DOID:0070399 | hypomyelinating leukodystrophy 18 | HGNC:13709 | Homo sapiens (human) | 8560 | DEGS1 |
|
||
| DOID:684 | hepatocellular carcinoma | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
|
||
| DOID:0111067 | congenital bile acid synthesis defect 6 | HGNC:120 | Homo sapiens (human) | 8309 | ACOX2 |
|
||
| DOID:0110798 | hereditary spastic paraplegia 46 | HGNC:18986 | Homo sapiens (human) | 57704 | GBA2 |
|
||
| DOID:12689 | acoustic neuroma | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
|
||
| DOID:12802 | mucopolysaccharidosis I | HGNC:5391 | Homo sapiens (human) | 3425 | IDUA |
|
