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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:10459 | common cold | HGNC:435 | Homo sapiens (human) | 240 | ALOX5 |
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| DOID:10652 | Alzheimer's disease | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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| DOID:9970 | obesity | HGNC:2615 | Homo sapiens (human) | 1555 | CYP2B6 |
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| DOID:11446 | sciatic neuropathy | HGNC:4243 | Homo sapiens (human) | 2674 | GFRA1 |
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| DOID:0070216 | familial hyperinsulinemic hypoglycemia 3 | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:1270 | hereditary hemorrhagic telangiectasia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:2043 | hepatitis B | HGNC:9053 | Homo sapiens (human) | 5329 | PLAUR |
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| DOID:114 | heart disease | HGNC:2591 | Homo sapiens (human) | 1584 | CYP11B1 |
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| DOID:10976 | membranous glomerulonephritis | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:12297 | Vogt-Koyanagi-Harada disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:3211 | lysosomal storage disease | HGNC:10933 | Homo sapiens (human) | 26503 | SLC17A5 |
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| DOID:13580 | cholestasis | HGNC:2651 | Homo sapiens (human) | 1581 | CYP7A1 |
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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:635 | acquired immunodeficiency syndrome | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:8986 | narcolepsy | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:3312 | bipolar disorder | HGNC:4092 | Homo sapiens (human) | 2571 | GAD1 |
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| DOID:12858 | Huntington's disease | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:27301 | Homo sapiens (human) | 200186 | CRTC2 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:6107 | Homo sapiens (human) | 3651 | PDX1 |
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| DOID:0080410 | familial adenomatous polyposis 2 | HGNC:7527 | Homo sapiens (human) | 4595 | MUTYH |
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| DOID:11168 | anogenital venereal wart | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:3594 | Homo sapiens (human) | 2194 | FASN |
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| DOID:3310 | atopic dermatitis | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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