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:0081168 | HMG-CoA synthase 2 deficiency | HGNC:5008 | Homo sapiens (human) | 3158 | HMGCS2 |
|
||
| DOID:9744 | type 1 diabetes mellitus | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
|
||
| DOID:12217 | Lewy body dementia | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
|
||
| DOID:2377 | multiple sclerosis | HGNC:4795 | Homo sapiens (human) | 9563 | H6PD |
|
||
| DOID:13141 | uveitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
|
||
| DOID:9455 | lipid storage disease | HGNC:9498 | Homo sapiens (human) | 5660 | PSAP |
|
||
| DOID:3454 | brain infarction | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
|
||
| DOID:1324 | lung cancer | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
|
||
| DOID:2476 | hereditary spastic paraplegia | HGNC:24768 | Homo sapiens (human) | 375775 | PNPLA7 |
|
||
| DOID:783 | end stage renal disease | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
|
||
| DOID:0112050 | non-syndromic X-linked intellectual disability 63 | HGNC:3570 | Homo sapiens (human) | 2181 | ACSL3 |
|
||
| DOID:5844 | myocardial infarction | HGNC:4617 | Homo sapiens (human) | 2932 | GSK3B |
|
||
| DOID:8719 | in situ carcinoma | HGNC:438 | Homo sapiens (human) | 249 | ALPL |
|
||
| DOID:6432 | pulmonary hypertension | HGNC:3402 | Homo sapiens (human) | 2053 | EPHX2 |
|
||
| DOID:3307 | teratoma | HGNC:8905 | Homo sapiens (human) | 5236 | PGM1 |
|
||
| DOID:631 | fibromyalgia | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
|
||
| DOID:0080556 | congenital disorder of glycosylation Id | HGNC:23056 | Homo sapiens (human) | 10195 | ALG3 |
|
||
| DOID:1586 | rheumatic fever | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
|
||
| DOID:684 | hepatocellular carcinoma | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
|
||
| DOID:5844 | myocardial infarction | HGNC:2597 | Homo sapiens (human) | 1545 | CYP1B1 |
|
||
| DOID:0111258 | pentosuria | HGNC:18985 | Homo sapiens (human) | 51181 | DCXR |
|
||
| DOID:784 | chronic kidney disease | HGNC:12663 | Homo sapiens (human) | 7412 | VCAM1 |
|
||
| DOID:0050563 | nonsyndromic deafness | HGNC:31088 | Homo sapiens (human) | 144245 | ALG10B |
|
||
| DOID:12549 | hepatitis A | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
|
||
| DOID:0070403 | hypomyelinating leukodystrophy 26 | HGNC:16872 | Homo sapiens (human) | 347734 | SLC35B2 |
|
