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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:0060071 | pre-malignant neoplasm | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0050642 | hypochromic microcytic anemia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:850 | lung disease | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:0050700 | cardiomyopathy | HGNC:18860 | Homo sapiens (human) | 56624 | ASAH2 |
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| DOID:1742 | drug psychosis | HGNC:4093 | Homo sapiens (human) | 2572 | GAD2 |
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| DOID:9268 | glycine encephalopathy | HGNC:4313 | Homo sapiens (human) | 2731 | GLDC |
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| DOID:3910 | lung adenocarcinoma | HGNC:5383 | Homo sapiens (human) | 3418 | IDH2 |
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| DOID:0070129 | autosomal recessive cutis laxa type IID | HGNC:851 | Homo sapiens (human) | 523 | ATP6V1A |
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| DOID:12930 | dilated cardiomyopathy | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:5813 | purine nucleoside phosphorylase deficiency | HGNC:7892 | Homo sapiens (human) | 4860 | PNP |
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| DOID:10871 | age related macular degeneration | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:3907 | lung squamous cell carcinoma | HGNC:5383 | Homo sapiens (human) | 3418 | IDH2 |
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| DOID:8778 | Crohn's disease | HGNC:429 | Homo sapiens (human) | 239 | ALOX12 |
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| DOID:10652 | Alzheimer's disease | HGNC:433 | Homo sapiens (human) | 246 | ALOX15 |
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| DOID:1826 | epilepsy | HGNC:25575 | Homo sapiens (human) | 55224 | ETNK2 |
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| DOID:9743 | diabetic neuropathy | HGNC:6876 | Homo sapiens (human) | 1432 | MAPK14 |
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| DOID:14701 | propionic acidemia | HGNC:8653 | Homo sapiens (human) | 5095 | PCCA |
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| DOID:10763 | hypertension | HGNC:9603 | Homo sapiens (human) | 5740 | PTGIS |
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| DOID:0080886 | vitamin D-dependent rickets type 1A | HGNC:2606 | Homo sapiens (human) | 1594 | CYP27B1 |
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| DOID:0111071 | congenital bile acid synthesis defect 1 | HGNC:18324 | Homo sapiens (human) | 80270 | HSD3B7 |
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| DOID:0050813 | spondyloepiphyseal dysplasia with congenital joint dislocations | HGNC:1971 | Homo sapiens (human) | 9469 | CHST3 |
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| DOID:0112072 | nuclear type mitochondrial complex I deficiency 20 | HGNC:88 | Homo sapiens (human) | 33 | ACADL |
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| DOID:0050912 | colon adenoma | HGNC:1937 | Homo sapiens (human) | 1119 | CHKA |
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| DOID:2738 | pseudoxanthoma elasticum | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:13241 | Behcet's disease | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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