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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:0050156 | idiopathic pulmonary fibrosis | HGNC:10799 | Homo sapiens (human) | 729238 | SFTPA2 |
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| DOID:11396 | pulmonary edema | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:9970 | obesity | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:11394 | adult respiratory distress syndrome | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:2957 | pulmonary tuberculosis | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:3082 | interstitial lung disease | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:841 | extrinsic allergic alveolitis | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:12120 | pulmonary alveolar proteinosis | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:12716 | newborn respiratory distress syndrome | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:0050127 | sinusitis | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:874 | bacterial pneumonia | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:3770 | pulmonary fibrosis | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| 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: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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