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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:684 | hepatocellular carcinoma | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:182 | calcinosis | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:0070262 | congenital disorder of glycosylation type IIj | HGNC:18620 | Homo sapiens (human) | 25839 | COG4 |
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| DOID:2596 | larynx cancer | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:2747 | glycogen storage disease | HGNC:9386 | Homo sapiens (human) | 51422 | PRKAG2 |
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| DOID:10825 | essential hypertension | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:2986 | IgA glomerulonephritis | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:5419 | schizophrenia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:4362 | cervical cancer | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0111234 | congenital muscular dystrophy-dystroglycanopathy A7 | HGNC:37276 | Homo sapiens (human) | 729920 | CRPPA |
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| DOID:3526 | cerebral infarction | HGNC:6623 | Homo sapiens (human) | 9388 | LIPG |
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| DOID:12205 | dengue disease | HGNC:1641 | Homo sapiens (human) | 30835 | CD209 |
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| DOID:9261 | nasopharynx carcinoma | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:8986 | narcolepsy | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:0080410 | familial adenomatous polyposis 2 | HGNC:7527 | Homo sapiens (human) | 4595 | MUTYH |
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| DOID:5204 | fructose-1,6-bisphosphatase deficiency | HGNC:3606 | Homo sapiens (human) | 2203 | FBP1 |
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| DOID:13832 | patent ductus arteriosus | HGNC:9603 | Homo sapiens (human) | 5740 | PTGIS |
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| DOID:9828 | neonatal abstinence syndrome | HGNC:2615 | Homo sapiens (human) | 1555 | CYP2B6 |
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| DOID:1324 | lung cancer | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:9256 | colorectal cancer | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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| DOID:2559 | opiate dependence | HGNC:7956 | Homo sapiens (human) | 4886 | NPY1R |
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| DOID:0080630 | B-lymphoblastic leukemia/lymphoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0080533 | Carney-Stratakis syndrome | HGNC:10681 | Homo sapiens (human) | 6390 | SDHB |
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| DOID:1909 | melanoma | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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