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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:2957 | pulmonary tuberculosis | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:3407 | carotid artery disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:552 | pneumonia | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:2986 | IgA glomerulonephritis | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:1205 | allergic disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:13580 | cholestasis | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:10608 | celiac disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:2945 | severe acute respiratory syndrome | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:11335 | sarcoidosis | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:5844 | myocardial infarction | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:10487 | Hirschsprung's disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:824 | periodontitis | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:898 | autosomal dominant polycystic kidney disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:13603 | obstructive jaundice | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:0070436 | hyperphosphatasia with impaired intellectual development syndrome 4 | HGNC:23719 | Homo sapiens (human) | 93210 | PGAP3 |
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| DOID:0050745 | diffuse large B-cell lymphoma | HGNC:1643 | Homo sapiens (human) | 933 | CD22 |
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| DOID:2377 | multiple sclerosis | HGNC:929 | Homo sapiens (human) | 9331 | B4GALT6 |
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| DOID:2377 | multiple sclerosis | HGNC:928 | Homo sapiens (human) | 9334 | B4GALT5 |
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| DOID:0060041 | autism spectrum disorder | HGNC:7682 | Homo sapiens (human) | 9348 | NDST3 |
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| DOID:14227 | azoospermia | HGNC:7682 | Homo sapiens (human) | 9348 | NDST3 |
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| DOID:1059 | intellectual disability | HGNC:7682 | Homo sapiens (human) | 9348 | NDST3 |
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| DOID:0081023 | retinal cone dystrophy 4 | HGNC:20202 | Homo sapiens (human) | 93589 | CACNA2D4 |
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| DOID:2247 | spondylosis | HGNC:6344 | Homo sapiens (human) | 9365 | KL |
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