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GlyTouCan
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
LM-GlycoRepo
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:418 | systemic scleroderma | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:13948 | bladder neck obstruction | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:12236 | primary biliary cholangitis | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:1474 | aggressive periodontitis | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:6432 | pulmonary hypertension | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:13359 | Ehlers-Danlos syndrome | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:5844 | myocardial infarction | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:4154 | dentinogenesis imperfecta | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:916 | liver benign neoplasm | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:12241 | beta thalassemia | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:13580 | cholestasis | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:11476 | osteoporosis | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:3507 | dermatofibrosarcoma protuberans | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:0080727 | Ehlers-Danlos syndrome arthrochalasia type 1 | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:12351 | alcoholic hepatitis | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:0080162 | lupus nephritis | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:0050827 | rheumatic heart disease | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:4257 | Caffey disease | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:0110339 | osteogenesis imperfecta type 3 | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:10808 | gastric ulcer | HGNC:2195 | Homo sapiens (human) | 80781 | COL18A1 |
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| DOID:0050700 | cardiomyopathy | HGNC:2195 | Homo sapiens (human) | 80781 | COL18A1 |
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| DOID:0060680 | pigment dispersion syndrome | HGNC:2195 | Homo sapiens (human) | 80781 | COL18A1 |
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| DOID:1405 | primary angle-closure glaucoma | HGNC:2195 | Homo sapiens (human) | 80781 | COL18A1 |
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