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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:9744 | type 1 diabetes mellitus | HGNC:1667 | Homo sapiens (human) | 952 | CD38 |
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| DOID:8778 | Crohn's disease | HGNC:10720 | Homo sapiens (human) | 6402 | SELL |
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| DOID:10652 | Alzheimer's disease | HGNC:4141 | Homo sapiens (human) | 2597 | GAPDH |
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| DOID:11724 | limb-girdle muscular dystrophy | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:3498 | pancreatic ductal adenocarcinoma | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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| DOID:3407 | carotid artery disease | HGNC:30092 | Homo sapiens (human) | 10135 | NAMPT |
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| DOID:2349 | arteriosclerosis | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:10763 | hypertension | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:4500 | hypokalemia | HGNC:381 | Homo sapiens (human) | 231 | AKR1B1 |
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| DOID:12858 | Huntington's disease | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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| DOID:10914 | amnestic disorder | HGNC:6126 | Homo sapiens (human) | 8660 | IRS2 |
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| DOID:326 | ischemia | HGNC:9599 | Homo sapiens (human) | 9536 | PTGES |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:3007 | Homo sapiens (human) | 54344 | DPM3 |
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| DOID:437 | myasthenia gravis | HGNC:108 | Homo sapiens (human) | 43 | ACHE |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:5998 | Homo sapiens (human) | 9173 | IL1RL1 |
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| DOID:3310 | atopic dermatitis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:2841 | asthma | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:10763 | hypertension | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:3459 | breast carcinoma | HGNC:2602 | Homo sapiens (human) | 1591 | CYP24A1 |
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| DOID:10283 | prostate cancer | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:0110937 | autosomal dominant osteopetrosis 1 | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:0050852 | limb ischemia | HGNC:9603 | Homo sapiens (human) | 5740 | PTGIS |
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| DOID:1168 | familial hyperlipidemia | HGNC:9989 | Homo sapiens (human) | 9104 | RGN |
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| DOID:576 | proteinuria | HGNC:7049 | Homo sapiens (human) | 4249 | MGAT5 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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