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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
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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:14557 | primary pulmonary hypertension | HGNC:9603 | Homo sapiens (human) | 5740 | PTGIS |
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| DOID:2316 | brain ischemia | HGNC:9603 | Homo sapiens (human) | 5740 | PTGIS |
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| DOID:6000 | congestive heart failure | HGNC:9603 | Homo sapiens (human) | 5740 | PTGIS |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:9603 | Homo sapiens (human) | 5740 | PTGIS |
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| DOID:14330 | Parkinson's disease | HGNC:9603 | Homo sapiens (human) | 5740 | PTGIS |
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| DOID:10763 | hypertension | HGNC:9603 | Homo sapiens (human) | 5740 | PTGIS |
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| DOID:0080491 | cerebral cavernous malformation 1 | HGNC:9603 | Homo sapiens (human) | 5740 | PTGIS |
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| DOID:0070254 | congenital disorder of glycosylation type IIb | MGI:1929872 | Mus musculus (house mouse) | 57377 | Mogs |
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| DOID:3407 | carotid artery disease | HGNC:9592 | Homo sapiens (human) | 5730 | PTGDS |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:9592 | Homo sapiens (human) | 5730 | PTGDS |
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| DOID:10003 | sensorineural hearing loss | HGNC:9592 | Homo sapiens (human) | 5730 | PTGDS |
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| DOID:10763 | hypertension | HGNC:9592 | Homo sapiens (human) | 5730 | PTGDS |
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| DOID:11664 | nephrosclerosis | HGNC:9592 | Homo sapiens (human) | 5730 | PTGDS |
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| DOID:9351 | diabetes mellitus | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:0060867 | macrocephaly-autism syndrome | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:13608 | biliary atresia | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:0014667 | disease of metabolism | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:8029 | sporadic breast cancer | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:5041 | esophageal cancer | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:8805 | intermediate coronary syndrome | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:4450 | renal cell carcinoma | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:1192 | peripheral nervous system neoplasm | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:219 | colon cancer | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:127 | leiomyoma | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:0080072 | intestinal pseudo-obstruction | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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