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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:321 | tropical spastic paraparesis | HGNC:18788 | Homo sapiens (human) | 22914 | KLRK1 |
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| DOID:10811 | nasal cavity cancer | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:1324 | lung cancer | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:824 | periodontitis | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:10534 | stomach cancer | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:890 | mitochondrial encephalomyopathy | HGNC:3148 | Homo sapiens (human) | 1890 | TYMP |
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| DOID:11836 | clubfoot | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:0050814 | temtamy preaxial brachydactyly syndrome | HGNC:17198 | Homo sapiens (human) | 22856 | CHSY1 |
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| DOID:2841 | asthma | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
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| DOID:0050742 | nicotine dependence | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
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| DOID:9008 | psoriatic arthritis | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:10652 | Alzheimer's disease | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:2349 | arteriosclerosis | HGNC:6021 | Homo sapiens (human) | 3572 | IL6ST |
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| DOID:0080283 | developmental and epileptic encephalopathy 55 | HGNC:3046 | Homo sapiens (human) | 51227 | PIGP |
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| DOID:0111105 | maturity-onset diabetes of the young type 8 | HGNC:1848 | Homo sapiens (human) | 1056 | CEL |
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| DOID:9119 | acute myeloid leukemia | HGNC:16496 | Homo sapiens (human) | 23305 | ACSL6 |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:0080132 | Sengers syndrome | HGNC:21869 | Homo sapiens (human) | 55750 | AGK |
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| DOID:4928 | intrahepatic cholangiocarcinoma | HGNC:5383 | Homo sapiens (human) | 3418 | IDH2 |
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| DOID:10591 | pre-eclampsia | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:0050628 | advanced sleep phase syndrome | HGNC:8846 | Homo sapiens (human) | 8864 | PER2 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:2615 | Homo sapiens (human) | 1555 | CYP2B6 |
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| DOID:0050083 | Keshan disease | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:0110294 | autosomal recessive limb-girdle muscular dystrophy type 2T | HGNC:22932 | Homo sapiens (human) | 29925 | GMPPB |
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