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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:12236 | primary biliary cholangitis | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:0050559 | Fukuyama congenital muscular dystrophy | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:11650 | bronchopulmonary dysplasia | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:3429 | inclusion body myositis | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:5844 | myocardial infarction | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:0110293 | autosomal recessive limb-girdle muscular dystrophy type 2P | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:767 | muscular atrophy | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:9884 | muscular dystrophy | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:0112374 | muscular dystrophy-dystroglycanopathy | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:0110278 | autosomal recessive limb-girdle muscular dystrophy type 2D | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:676 | juvenile rheumatoid arthritis | HGNC:26789 | Homo sapiens (human) | 144811 | LACC1 |
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| DOID:1936 | atherosclerosis | HGNC:26876 | Homo sapiens (human) | 165631 | PARP15 |
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| DOID:1826 | epilepsy | HGNC:26899 | Homo sapiens (human) | 160418 | TMTC3 |
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| DOID:0112233 | lissencephaly 8 | HGNC:26899 | Homo sapiens (human) | 160418 | TMTC3 |
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| DOID:9269 | maple syrup urine disease | HGNC:2698 | Homo sapiens (human) | 1629 | DBT |
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| DOID:12858 | Huntington's disease | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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| DOID:14330 | Parkinson's disease | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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| DOID:1074 | kidney failure | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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| DOID:848 | arthritis | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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| DOID:6000 | congestive heart failure | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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| DOID:5517 | stomach carcinoma | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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| DOID:224 | transient cerebral ischemia | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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| DOID:417 | autoimmune disease | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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