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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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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:0090080 | hypogonadotropic hypogonadism 16 with or without anosmia | HGNC:10723 | Homo sapiens (human) | 10371 | SEMA3A |
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| DOID:1825 | childhood absence epilepsy | HGNC:1406 | Homo sapiens (human) | 10369 | CACNG2 |
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| DOID:0070040 | autosomal dominant intellectual developmental disorder 10 | HGNC:1406 | Homo sapiens (human) | 10369 | CACNG2 |
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| DOID:5426 | primary ovarian insufficiency | HGNC:7930 | Homo sapiens (human) | 10361 | NPM2 |
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| DOID:700 | mitochondrial metabolism disease | HGNC:12730 | Homo sapiens (human) | 10352 | WARS2 |
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| DOID:0111364 | Alzheimer's disease 9 | HGNC:37 | Homo sapiens (human) | 10347 | ABCA7 |
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| DOID:0080385 | nephrotic syndrome type 11 | MGI:2143854 | Mus musculus (house mouse) | 103468 | Nup107 |
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| DOID:14450 | 46 XX gonadal dysgenesis | MGI:2143854 | Mus musculus (house mouse) | 103468 | Nup107 |
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| DOID:0080498 | ovarian dysgenesis 6 | MGI:2143854 | Mus musculus (house mouse) | 103468 | Nup107 |
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| DOID:0080694 | Galloway-Mowat syndrome | MGI:2143854 | Mus musculus (house mouse) | 103468 | Nup107 |
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| DOID:0060674 | catecholaminergic polymorphic ventricular tachycardia | HGNC:12261 | Homo sapiens (human) | 10345 | TRDN |
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| DOID:12930 | dilated cardiomyopathy | HGNC:12261 | Homo sapiens (human) | 10345 | TRDN |
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| DOID:0060679 | catecholaminergic polymorphic ventricular tachycardia 5 | HGNC:12261 | Homo sapiens (human) | 10345 | TRDN |
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| DOID:0110809 | hereditary spastic paraplegia 57 | HGNC:11758 | Homo sapiens (human) | 10342 | TFG |
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| DOID:4483 | rhinitis | HGNC:16711 | Homo sapiens (human) | 10333 | TLR6 |
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| DOID:8677 | perinatal necrotizing enterocolitis | HGNC:16711 | Homo sapiens (human) | 10333 | TLR6 |
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| DOID:13564 | aspergillosis | HGNC:16711 | Homo sapiens (human) | 10333 | TLR6 |
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| DOID:399 | tuberculosis | HGNC:16711 | Homo sapiens (human) | 10333 | TLR6 |
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| DOID:0060000 | infective endocarditis | HGNC:16711 | Homo sapiens (human) | 10333 | TLR6 |
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| DOID:2841 | asthma | HGNC:16711 | Homo sapiens (human) | 10333 | TLR6 |
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| DOID:874 | bacterial pneumonia | HGNC:16711 | Homo sapiens (human) | 10333 | TLR6 |
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| DOID:0050598 | extrapulmonary tuberculosis | HGNC:13523 | Homo sapiens (human) | 10332 | CLEC4M |
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| DOID:2957 | pulmonary tuberculosis | HGNC:13523 | Homo sapiens (human) | 10332 | CLEC4M |
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| DOID:2945 | severe acute respiratory syndrome | HGNC:13523 | Homo sapiens (human) | 10332 | CLEC4M |
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| DOID:0111239 | congenital muscular dystrophy-dystroglycanopathy type A10 | HGNC:13530 | Homo sapiens (human) | 10329 | RXYLT1 |
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