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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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Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▲ | References |
|---|---|---|---|---|---|---|---|---|
| DOID:5082 | liver cirrhosis | HGNC:3025 | Homo sapiens (human) | 1815 | DRD4 |
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| DOID:0050742 | nicotine dependence | HGNC:1964 | Homo sapiens (human) | 1143 | CHRNB4 |
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| DOID:11335 | sarcoidosis | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:4648 | familial retinoblastoma | HGNC:9884 | Homo sapiens (human) | 5925 | RB1 |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | HGNC:6554 | Homo sapiens (human) | 3953 | LEPR |
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| DOID:0110741 | type 1 diabetes mellitus 2 | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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| DOID:12177 | common variable immunodeficiency | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:10892 | hypospadias | HGNC:2568 | Homo sapiens (human) | 10046 | MAMLD1 |
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| DOID:14735 | hereditary angioedema | HGNC:3656 | Homo sapiens (human) | 26509 | MYOF |
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| DOID:10283 | prostate cancer | HGNC:7652 | Homo sapiens (human) | 4683 | NBN |
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| DOID:0060532 | latex allergy | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:10652 | Alzheimer's disease | HGNC:602 | Homo sapiens (human) | 337 | APOA4 |
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| DOID:3312 | bipolar disorder | HGNC:4617 | Homo sapiens (human) | 2932 | GSK3B |
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| DOID:11612 | polycystic ovary syndrome | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:0070143 | autosomal recessive cutis laxa type III | HGNC:9722 | Homo sapiens (human) | 5832 | ALDH18A1 |
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| DOID:1324 | lung cancer | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:7575 | pancreatic intraductal papillary-mucinous neoplasm | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:9452 | steatotic liver disease | HGNC:4886 | Homo sapiens (human) | 3077 | HFE |
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| DOID:4990 | essential tremor | HGNC:6893 | Homo sapiens (human) | 4137 | MAPT |
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| DOID:2377 | multiple sclerosis | HGNC:8760 | Homo sapiens (human) | 5133 | PDCD1 |
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| DOID:0050431 | arrhythmogenic right ventricular cardiomyopathy | HGNC:3052 | Homo sapiens (human) | 1832 | DSP |
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| DOID:0111118 | nephronophthisis 11 | HGNC:28396 | Homo sapiens (human) | 91147 | TMEM67 |
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| DOID:0110978 | brachydactyly type A1D | HGNC:1077 | Homo sapiens (human) | 658 | BMPR1B |
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| DOID:10652 | Alzheimer's disease | HGNC:8724 | Homo sapiens (human) | 5105 | PCK1 |
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| DOID:0060496 | respiratory allergy | HGNC:5973 | Homo sapiens (human) | 3596 | IL13 |
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