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GlyTouCan
Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
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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:0050830 | peripheral artery disease | HGNC:7956 | Homo sapiens (human) | 4886 | NPY1R |
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| DOID:224 | transient cerebral ischemia | HGNC:18451 | Homo sapiens (human) | 90411 | MCFD2 |
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| DOID:3963 | thyroid gland carcinoma | HGNC:15855 | Homo sapiens (human) | 22918 | CD93 |
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| DOID:0050589 | inflammatory bowel disease | HGNC:23614 | Homo sapiens (human) | 55808 | ST6GALNAC1 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:20266 | Homo sapiens (human) | 29880 | ALG5 |
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| DOID:0070254 | congenital disorder of glycosylation type IIb | HGNC:24862 | Homo sapiens (human) | 7841 | MOGS |
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| DOID:824 | periodontitis | HGNC:3774 | Homo sapiens (human) | 2331 | FMOD |
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| DOID:10591 | pre-eclampsia | HGNC:2634 | Homo sapiens (human) | 1573 | CYP2J2 |
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| DOID:0050848 | obstructive sleep apnea | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:11204 | allergic conjunctivitis | HGNC:9031 | Homo sapiens (human) | 5320 | PLA2G2A |
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| DOID:12930 | dilated cardiomyopathy | HGNC:9922 | Homo sapiens (human) | 5950 | RBP4 |
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| DOID:1793 | pancreatic cancer | HGNC:251 | Homo sapiens (human) | 126 | ADH1C |
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| DOID:2377 | multiple sclerosis | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:1287 | cardiovascular system disease | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:635 | acquired immunodeficiency syndrome | HGNC:1641 | Homo sapiens (human) | 30835 | CD209 |
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| DOID:0080599 | Coronavirus infectious disease | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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| DOID:162 | cancer | HGNC:9640 | Homo sapiens (human) | 201562 | HACD2 |
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| DOID:1184 | nephrotic syndrome | HGNC:25223 | Homo sapiens (human) | 27235 | COQ2 |
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| DOID:1612 | breast cancer | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:684 | hepatocellular carcinoma | HGNC:9989 | Homo sapiens (human) | 9104 | RGN |
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| DOID:0112250 | Gaucher's disease type IIIC | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:6000 | congestive heart failure | HGNC:9060 | Homo sapiens (human) | 5333 | PLCD1 |
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| DOID:0070218 | familial hyperinsulinemic hypoglycemia 2 | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:11612 | polycystic ovary syndrome | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:9538 | multiple myeloma | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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