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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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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MIRAGE
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:12365 | malaria | HGNC:17760 | Homo sapiens (human) | 54210 | TREM1 |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:17760 | Homo sapiens (human) | 54210 | TREM1 |
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| DOID:9120 | amyloidosis | HGNC:17760 | Homo sapiens (human) | 54210 | TREM1 |
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||
| DOID:1883 | hepatitis C | HGNC:17760 | Homo sapiens (human) | 54210 | TREM1 |
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| DOID:5844 | myocardial infarction | HGNC:17760 | Homo sapiens (human) | 54210 | TREM1 |
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||
| DOID:2043 | hepatitis B | HGNC:17760 | Homo sapiens (human) | 54210 | TREM1 |
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||
| DOID:6000 | congestive heart failure | HGNC:17760 | Homo sapiens (human) | 54210 | TREM1 |
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| DOID:1596 | depressive disorder | HGNC:17760 | Homo sapiens (human) | 54210 | TREM1 |
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| DOID:3525 | middle cerebral artery infarction | HGNC:17760 | Homo sapiens (human) | 54210 | TREM1 |
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| DOID:7148 | rheumatoid arthritis | HGNC:17760 | Homo sapiens (human) | 54210 | TREM1 |
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| DOID:14115 | toxic shock syndrome | HGNC:17760 | Homo sapiens (human) | 54210 | TREM1 |
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| DOID:0050697 | chorioamnionitis | HGNC:17760 | Homo sapiens (human) | 54210 | TREM1 |
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| DOID:9255 | frontotemporal dementia | HGNC:17761 | Homo sapiens (human) | 54209 | TREM2 |
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| DOID:4166 | syphilis | HGNC:17761 | Homo sapiens (human) | 54209 | TREM2 |
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| DOID:0050593 | primary congenital glaucoma | HGNC:1778 | Homo sapiens (human) | 1022 | CDK7 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:1778 | Homo sapiens (human) | 1022 | CDK7 |
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| DOID:1612 | breast cancer | HGNC:1778 | Homo sapiens (human) | 1022 | CDK7 |
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| DOID:0110965 | brachydactyly type A2 | HGNC:1778 | Homo sapiens (human) | 1022 | CDK7 |
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| DOID:10652 | Alzheimer's disease | HGNC:1778 | Homo sapiens (human) | 1022 | CDK7 |
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| DOID:10825 | essential hypertension | HGNC:1778 | Homo sapiens (human) | 1022 | CDK7 |
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| DOID:9993 | hypoglycemia | HGNC:1778 | Homo sapiens (human) | 1022 | CDK7 |
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| DOID:13099 | Moyamoya disease | HGNC:17780 | Homo sapiens (human) | 345651 | ACTBL2 |
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| DOID:10486 | intestinal atresia | HGNC:17780 | Homo sapiens (human) | 345651 | ACTBL2 |
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| DOID:0081112 | Baraitser-Winter syndrome 1 | HGNC:17780 | Homo sapiens (human) | 345651 | ACTBL2 |
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| DOID:0110550 | autosomal dominant nonsyndromic deafness 20 | HGNC:17780 | Homo sapiens (human) | 345651 | ACTBL2 |
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