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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:13241 | Behcet's disease | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:3312 | bipolar disorder | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
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| DOID:4195 | hyperglycemia | HGNC:5273 | Homo sapiens (human) | 3339 | HSPG2 |
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| DOID:12849 | autistic disorder | HGNC:10982 | Homo sapiens (human) | 8604 | SLC25A12 |
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| DOID:11983 | Prader-Willi syndrome | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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| DOID:3393 | coronary artery disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:1612 | breast cancer | HGNC:545 | Homo sapiens (human) | 310 | ANXA7 |
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| DOID:13241 | Behcet's disease | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:10584 | retinitis pigmentosa | HGNC:1375 | Homo sapiens (human) | 762 | CA4 |
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| DOID:657 | adenoma | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
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| DOID:1612 | breast cancer | HGNC:2665 | Homo sapiens (human) | 1604 | CD55 |
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| DOID:630 | genetic disease | HGNC:18622 | Homo sapiens (human) | 91949 | COG7 |
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| DOID:10652 | Alzheimer's disease | HGNC:433 | Homo sapiens (human) | 246 | ALOX15 |
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| DOID:4481 | allergic rhinitis | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:3393 | coronary artery disease | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
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| DOID:0060639 | permanent neonatal diabetes mellitus | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:9008 | psoriatic arthritis | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:10652 | Alzheimer's disease | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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| DOID:0050697 | chorioamnionitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:5844 | myocardial infarction | HGNC:6562 | Homo sapiens (human) | 3957 | LGALS2 |
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| DOID:11132 | prostatic hypertrophy | HGNC:11284 | Homo sapiens (human) | 6715 | SRD5A1 |
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| DOID:5844 | myocardial infarction | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:3649 | pyruvate decarboxylase deficiency | HGNC:8808 | Homo sapiens (human) | 5162 | PDHB |
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| DOID:13378 | Kawasaki disease | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:0050570 | congenital disorder of glycosylation type I | SGD:S000005163 | Saccharomyces cerevisiae S288C | 855502 | ALG9 |
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