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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:12894 | Sjogren's syndrome | HGNC:15582 | Homo sapiens (human) | 94025 | MUC16 |
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| DOID:9368 | keratoconjunctivitis | HGNC:15582 | Homo sapiens (human) | 94025 | MUC16 |
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| DOID:4001 | ovarian carcinoma | HGNC:15582 | Homo sapiens (human) | 94025 | MUC16 |
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| DOID:10652 | Alzheimer's disease | MGI:2137022 | Mus musculus (house mouse) | 94043 | Tm2d1 |
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| DOID:3213 | demyelinating disease | HGNC:1700 | Homo sapiens (human) | 941 | CD80 |
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| DOID:7148 | rheumatoid arthritis | HGNC:1700 | Homo sapiens (human) | 941 | CD80 |
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| DOID:4780 | anti-basement membrane glomerulonephritis | HGNC:1700 | Homo sapiens (human) | 941 | CD80 |
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| DOID:3070 | high grade glioma | HGNC:1700 | Homo sapiens (human) | 941 | CD80 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:1700 | Homo sapiens (human) | 941 | CD80 |
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| DOID:1074 | kidney failure | HGNC:1700 | Homo sapiens (human) | 941 | CD80 |
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| DOID:0050523 | adult T-cell leukemia/lymphoma | HGNC:1700 | Homo sapiens (human) | 941 | CD80 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:1700 | Homo sapiens (human) | 941 | CD80 |
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| DOID:9074 | systemic lupus erythematosus | HGNC:1700 | Homo sapiens (human) | 941 | CD80 |
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| DOID:3388 | periodontal disease | HGNC:1700 | Homo sapiens (human) | 941 | CD80 |
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| DOID:2378 | relapsing-remitting multiple sclerosis | HGNC:1700 | Homo sapiens (human) | 941 | CD80 |
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| DOID:2841 | asthma | HGNC:16036 | Homo sapiens (human) | 94101 | ORMDL1 |
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| DOID:5419 | schizophrenia | MGI:2137383 | Mus musculus (house mouse) | 94109 | Csmd1 |
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| DOID:5419 | schizophrenia | MGI:2137379 | Mus musculus (house mouse) | 94112 | Med15 |
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| DOID:0060413 | chromosome 22q11.2 deletion syndrome, distal | MGI:2137379 | Mus musculus (house mouse) | 94112 | Med15 |
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| DOID:0050578 | occult macular dystrophy | HGNC:15946 | Homo sapiens (human) | 94137 | RP1L1 |
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| DOID:0112145 | retinitis pigmentosa 88 | HGNC:15946 | Homo sapiens (human) | 94137 | RP1L1 |
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| DOID:5614 | eye disease | HGNC:15946 | Homo sapiens (human) | 94137 | RP1L1 |
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| DOID:10763 | hypertension | HGNC:11828 | Homo sapiens (human) | 9414 | TJP2 |
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| DOID:0070224 | progressive familial intrahepatic cholestasis 4 | HGNC:11828 | Homo sapiens (human) | 9414 | TJP2 |
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| DOID:0014667 | disease of metabolism | HGNC:11828 | Homo sapiens (human) | 9414 | TJP2 |
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