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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:552 | pneumonia | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:1273 | respiratory syncytial virus infectious disease | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:2841 | asthma | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:11650 | bronchopulmonary dysplasia | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:13406 | pulmonary sarcoidosis | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:3827 | congenital diaphragmatic hernia | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:850 | lung disease | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:1485 | cystic fibrosis | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:9970 | obesity | HGNC:18359 | Homo sapiens (human) | 145264 | SERPINA12 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:18359 | Homo sapiens (human) | 145264 | SERPINA12 |
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| DOID:13372 | alpha 1-antitrypsin deficiency | HGNC:18359 | Homo sapiens (human) | 145264 | SERPINA12 |
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| DOID:0070221 | progressive familial intrahepatic cholestasis | HGNC:10741 | Homo sapiens (human) | 8482 | SEMA7A |
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| DOID:10652 | Alzheimer's disease | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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| DOID:3310 | atopic dermatitis | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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| DOID:1936 | atherosclerosis | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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| DOID:0080998 | acute necrotizing pancreatitis | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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| DOID:8577 | ulcerative colitis | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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| DOID:13378 | Kawasaki disease | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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| DOID:676 | juvenile rheumatoid arthritis | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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| DOID:8805 | intermediate coronary syndrome | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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| DOID:0060180 | colitis | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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| DOID:12894 | Sjogren's syndrome | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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| DOID:4780 | anti-basement membrane glomerulonephritis | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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