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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
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:0112314 | brain small vessel disease 2 | HGNC:2203 | Homo sapiens (human) | 1284 | COL4A2 |
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| DOID:0080000 | muscular disease | HGNC:2330 | Homo sapiens (human) | 1376 | CPT2 |
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| DOID:0080653 | urolithiasis | HGNC:9052 | Homo sapiens (human) | 5328 | PLAU |
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| DOID:10159 | osteonecrosis | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:14766 | renal agenesis | HGNC:6144 | Homo sapiens (human) | 8516 | ITGA8 |
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| DOID:0111542 | familial expansile osteolysis | HGNC:11908 | Homo sapiens (human) | 8792 | TNFRSF11A |
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| DOID:1059 | intellectual disability | HGNC:30237 | Homo sapiens (human) | 54862 | CC2D1A |
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| DOID:1441 | autosomal dominant cerebellar ataxia | HGNC:7952 | Homo sapiens (human) | 4884 | NPTX1 |
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| DOID:639 | acute disseminated encephalomyelitis | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:3717 | gastric adenocarcinoma | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:0110340 | osteogenesis imperfecta type 4 | HGNC:2198 | Homo sapiens (human) | 1278 | COL1A2 |
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| DOID:2526 | prostate adenocarcinoma | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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| DOID:0060193 | amyotrophic lateral sclerosis type 1 | HGNC:2711 | Homo sapiens (human) | 1639 | DCTN1 |
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| DOID:3907 | lung squamous cell carcinoma | HGNC:9673 | Homo sapiens (human) | 5795 | PTPRJ |
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| DOID:8778 | Crohn's disease | HGNC:5331 | Homo sapiens (human) | 64127 | NOD2 |
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| DOID:655 | inherited metabolic disorder | HGNC:6598 | Homo sapiens (human) | 3978 | LIG1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:1512 | Homo sapiens (human) | 844 | CASQ1 |
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| DOID:3490 | Noonan syndrome | HGNC:9829 | Homo sapiens (human) | 5894 | RAF1 |
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| DOID:891 | progressive myoclonus epilepsy | HGNC:3413 | Homo sapiens (human) | 7957 | EPM2A |
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| DOID:6420 | pulmonary valve stenosis | HGNC:11187 | Homo sapiens (human) | 6654 | SOS1 |
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| DOID:0080952 | AMED syndrome | HGNC:253 | Homo sapiens (human) | 128 | ADH5 |
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| DOID:13141 | uveitis | HGNC:19100 | Homo sapiens (human) | 149233 | IL23R |
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| DOID:10584 | retinitis pigmentosa | HGNC:2148 | Homo sapiens (human) | 1259 | CNGA1 |
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| DOID:0110262 | cataract 45 | HGNC:23801 | Homo sapiens (human) | 23094 | SIPA1L3 |
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| DOID:2841 | asthma | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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