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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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID ▼ | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:9119 | acute myeloid leukemia | HGNC:7669 | Homo sapiens (human) | 10499 | NCOA2 |
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| DOID:2526 | prostate adenocarcinoma | HGNC:7669 | Homo sapiens (human) | 10499 | NCOA2 |
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| DOID:10283 | prostate cancer | HGNC:7669 | Homo sapiens (human) | 10499 | NCOA2 |
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| DOID:0080199 | colorectal carcinoma | HGNC:7669 | Homo sapiens (human) | 10499 | NCOA2 |
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| DOID:11612 | polycystic ovary syndrome | HGNC:7669 | Homo sapiens (human) | 10499 | NCOA2 |
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| DOID:1574 | alcohol use disorder | HGNC:12566 | Homo sapiens (human) | 10497 | UNC13B |
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| DOID:1826 | epilepsy | HGNC:12566 | Homo sapiens (human) | 10497 | UNC13B |
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| DOID:0110337 | osteogenesis imperfecta type 7 | HGNC:2379 | Homo sapiens (human) | 10491 | CRTAP |
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| DOID:0050696 | fetal alcohol spectrum disorder | HGNC:51483 | Homo sapiens (human) | 104909134 | LINC02210-CRHR1 |
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| DOID:9778 | irritable bowel syndrome | HGNC:51483 | Homo sapiens (human) | 104909134 | LINC02210-CRHR1 |
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| DOID:12918 | thromboangiitis obliterans | HGNC:51483 | Homo sapiens (human) | 104909134 | LINC02210-CRHR1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:51483 | Homo sapiens (human) | 104909134 | LINC02210-CRHR1 |
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| DOID:3877 | functional colonic disease | HGNC:51483 | Homo sapiens (human) | 104909134 | LINC02210-CRHR1 |
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| DOID:10763 | hypertension | HGNC:51483 | Homo sapiens (human) | 104909134 | LINC02210-CRHR1 |
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| DOID:1596 | depressive disorder | HGNC:51483 | Homo sapiens (human) | 104909134 | LINC02210-CRHR1 |
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| DOID:1793 | pancreatic cancer | HGNC:20040 | Homo sapiens (human) | 10487 | CAP1 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:20039 | Homo sapiens (human) | 10486 | CAP2 |
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| DOID:5325 | Roberts syndrome | HGNC:10701 | Homo sapiens (human) | 10484 | SEC23A |
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| DOID:0111401 | congenital dyserythropoietic anemia type II | HGNC:10701 | Homo sapiens (human) | 10484 | SEC23A |
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| DOID:0070307 | craniolenticulosutural dysplasia | HGNC:10701 | Homo sapiens (human) | 10484 | SEC23A |
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| DOID:0081003 | Cowden syndrome 7 | HGNC:10702 | Homo sapiens (human) | 10483 | SEC23B |
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| DOID:0070307 | craniolenticulosutural dysplasia | HGNC:10702 | Homo sapiens (human) | 10483 | SEC23B |
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| DOID:0111401 | congenital dyserythropoietic anemia type II | HGNC:10702 | Homo sapiens (human) | 10483 | SEC23B |
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| DOID:5325 | Roberts syndrome | HGNC:10702 | Homo sapiens (human) | 10483 | SEC23B |
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| DOID:0060825 | Christianson syndrome | HGNC:11079 | Homo sapiens (human) | 10479 | SLC9A6 |
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