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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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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:1380 | endometrial cancer | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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| DOID:9743 | diabetic neuropathy | RGD:3734 | Rattus norvegicus (Norway rat) | 24788 | Sord |
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| DOID:5138 | leiomyomatosis | HGNC:1681 | Homo sapiens (human) | 960 | CD44 |
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| DOID:13406 | pulmonary sarcoidosis | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:2945 | severe acute respiratory syndrome | HGNC:79 | Homo sapiens (human) | 28 | ABO |
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| DOID:4247 | coronary restenosis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:1459 | hypothyroidism | RGD:631339 | Rattus norvegicus (Norway rat) | 288583 | Plod3 |
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| DOID:1459 | hypothyroidism | RGD:620330 | Rattus norvegicus (Norway rat) | 170587 | Cs |
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| DOID:7998 | hyperthyroidism | RGD:620330 | Rattus norvegicus (Norway rat) | 170587 | Cs |
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| DOID:4448 | macular degeneration | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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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:12930 | dilated cardiomyopathy | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:12206 | dengue hemorrhagic fever | HGNC:1641 | Homo sapiens (human) | 30835 | CD209 |
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| DOID:705 | Leber hereditary optic neuropathy | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0080599 | Coronavirus infectious disease | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:2671 | transitional cell carcinoma | HGNC:3148 | Homo sapiens (human) | 1890 | TYMP |
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| DOID:14330 | Parkinson's disease | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:678 | progressive supranuclear palsy | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:4450 | renal cell carcinoma | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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| DOID:1407 | anterior uveitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0080855 | Parkinsonism | RGD:69247 | Rattus norvegicus (Norway rat) | 83535 | Kcnj11 |
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| DOID:5844 | myocardial infarction | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:9368 | keratoconjunctivitis | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:2747 | glycogen storage disease | HGNC:9386 | Homo sapiens (human) | 51422 | PRKAG2 |
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| DOID:0080016 | spina bifida | HGNC:587 | Homo sapiens (human) | 328 | APEX1 |
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