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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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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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:12689 | acoustic neuroma | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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| DOID:1574 | alcohol use disorder | HGNC:3025 | Homo sapiens (human) | 1815 | DRD4 |
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| DOID:0110206 | Charcot-Marie-Tooth disease dominant intermediate F | HGNC:20731 | Homo sapiens (human) | 59345 | GNB4 |
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| DOID:10584 | retinitis pigmentosa | HGNC:9462 | Homo sapiens (human) | 5631 | PRPS1 |
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| DOID:5041 | esophageal cancer | HGNC:11896 | Homo sapiens (human) | 7128 | TNFAIP3 |
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| DOID:5844 | myocardial infarction | HGNC:3535 | Homo sapiens (human) | 2147 | F2 |
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| DOID:0090145 | dopamine beta-hydroxylase deficiency | HGNC:5238 | Homo sapiens (human) | 3309 | HSPA5 |
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| DOID:676 | juvenile rheumatoid arthritis | HGNC:7067 | Homo sapiens (human) | 4261 | CIITA |
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| DOID:1909 | melanoma | HGNC:6693 | Homo sapiens (human) | 53353 | LRP1B |
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| DOID:3407 | carotid artery disease | HGNC:9236 | Homo sapiens (human) | 5468 | PPARG |
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| DOID:0111995 | immunodeficiency 28 | HGNC:5440 | Homo sapiens (human) | 3460 | IFNGR2 |
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| DOID:2957 | pulmonary tuberculosis | HGNC:43 | Homo sapiens (human) | 6890 | TAP1 |
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| DOID:12185 | otosclerosis | HGNC:333 | Homo sapiens (human) | 183 | AGT |
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| DOID:0112315 | brain small vessel disease 3 | HGNC:26182 | Homo sapiens (human) | 79709 | COLGALT1 |
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| DOID:0080862 | primary ovarian insufficiency 5 | HGNC:22448 | Homo sapiens (human) | 135935 | NOBOX |
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| DOID:13001 | carotid stenosis | HGNC:3535 | Homo sapiens (human) | 2147 | F2 |
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| DOID:0080230 | autosomal dominant intellectual developmental disorder 54 | HGNC:1461 | Homo sapiens (human) | 816 | CAMK2B |
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| DOID:3070 | high grade glioma | HGNC:29832 | Homo sapiens (human) | 55191 | NADSYN1 |
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| DOID:0080283 | developmental and epileptic encephalopathy 55 | HGNC:3046 | Homo sapiens (human) | 51227 | PIGP |
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| DOID:0111070 | congenital bile acid synthesis defect 3 | HGNC:2652 | Homo sapiens (human) | 9420 | CYP7B1 |
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| DOID:0080238 | autosomal dominant intellectual developmental disorder 47 | HGNC:11354 | Homo sapiens (human) | 10274 | STAG1 |
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| DOID:11678 | onchocerciasis | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:0070304 | multiple epiphyseal dysplasia 3 | HGNC:2219 | Homo sapiens (human) | 1299 | COL9A3 |
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| DOID:0060841 | isolated microphthalmia 8 | HGNC:409 | Homo sapiens (human) | 220 | ALDH1A3 |
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| DOID:11963 | esophagitis | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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