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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:6000 | congestive heart failure | HGNC:9068 | Homo sapiens (human) | 5338 | PLD2 |
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| DOID:684 | hepatocellular carcinoma | HGNC:9065 | Homo sapiens (human) | 5335 | PLCG1 |
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| DOID:1993 | rectum cancer | HGNC:6876 | Homo sapiens (human) | 1432 | MAPK14 |
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| DOID:7188 | autoimmune thyroiditis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:6432 | pulmonary hypertension | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:11054 | urinary bladder cancer | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:9970 | obesity | HGNC:429 | Homo sapiens (human) | 239 | ALOX12 |
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| DOID:5844 | myocardial infarction | HGNC:2422 | Homo sapiens (human) | 1431 | CS |
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| DOID:850 | lung disease | HGNC:10802 | Homo sapiens (human) | 6440 | SFTPC |
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| DOID:2377 | multiple sclerosis | HGNC:30308 | Homo sapiens (human) | 56963 | RGMA |
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| DOID:2211 | factor XIII deficiency | HGNC:6631 | Homo sapiens (human) | 3998 | LMAN1 |
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| DOID:0050700 | cardiomyopathy | HGNC:10680 | Homo sapiens (human) | 6389 | SDHA |
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| DOID:0110790 | hereditary spastic paraplegia 39 | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:11963 | esophagitis | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:0050560 | Walker-Warburg syndrome | HGNC:13530 | Homo sapiens (human) | 10329 | RXYLT1 |
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| DOID:0080561 | congenital disorder of glycosylation Ii | HGNC:23159 | Homo sapiens (human) | 85365 | ALG2 |
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| DOID:1184 | nephrotic syndrome | HGNC:24865 | Homo sapiens (human) | 57678 | GPAM |
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| DOID:0050439 | Usher syndrome | HGNC:24102 | Homo sapiens (human) | 22901 | ARSG |
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| DOID:0080718 | GNE myopathy | HGNC:23657 | Homo sapiens (human) | 10020 | GNE |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:4456 | Homo sapiens (human) | 2820 | GPD2 |
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| DOID:12236 | primary biliary cholangitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:9452 | steatotic liver disease | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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| DOID:0090032 | Silverman-Handmaker type dyssegmental dysplasia | HGNC:5273 | Homo sapiens (human) | 3339 | HSPG2 |
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| DOID:3307 | teratoma | HGNC:8907 | Homo sapiens (human) | 5238 | PGM3 |
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