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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:8893 | psoriasis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:219 | colon cancer | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:0081120 | Graves ophthalmopathy | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:10534 | stomach cancer | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:2642 | Homo sapiens (human) | 1579 | CYP4A11 |
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| DOID:783 | end stage renal disease | HGNC:2638 | Homo sapiens (human) | 1577 | CYP3A5 |
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| DOID:635 | acquired immunodeficiency syndrome | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:8970 | subacute sclerosing panencephalitis | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:12930 | dilated cardiomyopathy | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:1206 | Rett syndrome | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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| DOID:0080600 | COVID-19 | HGNC:10718 | Homo sapiens (human) | 6401 | SELE |
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| DOID:3393 | coronary artery disease | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:14497 | Wolman disease | HGNC:6617 | Homo sapiens (human) | 3988 | LIPA |
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| DOID:684 | hepatocellular carcinoma | HGNC:2621 | Homo sapiens (human) | 1557 | CYP2C19 |
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| DOID:7693 | abdominal aortic aneurysm | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:0060074 | ductal carcinoma in situ | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0110444 | dilated cardiomyopathy 1X | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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| DOID:0112237 | lissencephaly 1 | HGNC:8574 | Homo sapiens (human) | 5048 | PAFAH1B1 |
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| DOID:11247 | disseminated intravascular coagulation | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:12541 | Homo sapiens (human) | 54600 | UGT1A9 |
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| DOID:0080379 | nephrotic syndrome type 2 | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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| DOID:3132 | porphyria cutanea tarda | HGNC:2596 | Homo sapiens (human) | 1544 | CYP1A2 |
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| DOID:3525 | middle cerebral artery infarction | HGNC:4341 | Homo sapiens (human) | 2752 | GLUL |
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| DOID:0110479 | autosomal recessive nonsyndromic deafness 21 | HGNC:11720 | Homo sapiens (human) | 7007 | TECTA |
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