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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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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:3910 | lung adenocarcinoma | HGNC:14129 | Homo sapiens (human) | 10919 | EHMT2 |
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| DOID:0060352 | Kleefstra syndrome 1 | HGNC:14129 | Homo sapiens (human) | 10919 | EHMT2 |
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| DOID:0050696 | fetal alcohol spectrum disorder | HGNC:14129 | Homo sapiens (human) | 10919 | EHMT2 |
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| DOID:986 | alopecia areata | HGNC:14129 | Homo sapiens (human) | 10919 | EHMT2 |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:14129 | Homo sapiens (human) | 10919 | EHMT2 |
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| DOID:934 | viral infectious disease | HGNC:14129 | Homo sapiens (human) | 10919 | EHMT2 |
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| DOID:0050156 | idiopathic pulmonary fibrosis | HGNC:14129 | Homo sapiens (human) | 10919 | EHMT2 |
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| DOID:0081423 | familial focal epilepsy with variable foci 3 | HGNC:14124 | Homo sapiens (human) | 8131 | NPRL3 |
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| DOID:2476 | hereditary spastic paraplegia | HGNC:14085 | Homo sapiens (human) | 57142 | RTN4 |
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| DOID:11832 | visual epilepsy | HGNC:14085 | Homo sapiens (human) | 57142 | RTN4 |
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| DOID:0110765 | hereditary spastic paraplegia 12 | HGNC:14085 | Homo sapiens (human) | 57142 | RTN4 |
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| DOID:0111133 | focal segmental glomerulosclerosis 8 | HGNC:14082 | Homo sapiens (human) | 54443 | ANLN |
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| DOID:9408 | acute myocardial infarction | HGNC:1408 | Homo sapiens (human) | 27092 | CACNG4 |
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| DOID:5409 | lung small cell carcinoma | HGNC:14079 | Homo sapiens (human) | 55584 | CHRNA9 |
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| DOID:0111954 | immunodeficiency 60 | HGNC:14078 | Homo sapiens (human) | 60468 | BACH2 |
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| DOID:11446 | sciatic neuropathy | HGNC:14076 | Homo sapiens (human) | 29956 | CERS2 |
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| DOID:9884 | muscular dystrophy | HGNC:14075 | Homo sapiens (human) | 137868 | SGCZ |
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| DOID:0050700 | cardiomyopathy | HGNC:14075 | Homo sapiens (human) | 137868 | SGCZ |
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| DOID:0110436 | dilated cardiomyopathy 1L | HGNC:14075 | Homo sapiens (human) | 137868 | SGCZ |
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| DOID:986 | alopecia areata | HGNC:14067 | Homo sapiens (human) | 51564 | HDAC7 |
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| DOID:9256 | colorectal cancer | HGNC:14067 | Homo sapiens (human) | 51564 | HDAC7 |
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| DOID:3525 | middle cerebral artery infarction | HGNC:14065 | Homo sapiens (human) | 9734 | HDAC9 |
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| DOID:9970 | obesity | HGNC:14064 | Homo sapiens (human) | 10013 | HDAC6 |
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| DOID:10763 | hypertension | HGNC:14064 | Homo sapiens (human) | 10013 | HDAC6 |
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| DOID:14330 | Parkinson's disease | HGNC:14064 | Homo sapiens (human) | 10013 | HDAC6 |
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