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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:0080946 | retinal dystrophy with leukodystrophy | HGNC:23338 | Homo sapiens (human) | 91452 | ACBD5 |
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| DOID:906 | peroxisomal disease | HGNC:23338 | Homo sapiens (human) | 91452 | ACBD5 |
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| DOID:870 | neuropathy | HGNC:10663 | Homo sapiens (human) | 9147 | NEMF |
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| DOID:440 | neuromuscular disease | HGNC:10663 | Homo sapiens (human) | 9147 | NEMF |
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| DOID:627 | severe combined immunodeficiency | HGNC:1673 | Homo sapiens (human) | 915 | CD3D |
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| DOID:0111972 | immunodeficiency 19 | HGNC:1673 | Homo sapiens (human) | 915 | CD3D |
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| DOID:0060698 | hyperekplexia 3 | HGNC:11051 | Homo sapiens (human) | 9152 | SLC6A5 |
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| DOID:11723 | Duchenne muscular dystrophy | HGNC:11051 | Homo sapiens (human) | 9152 | SLC6A5 |
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| DOID:5426 | primary ovarian insufficiency | HGNC:3511 | Homo sapiens (human) | 9156 | EXO1 |
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| DOID:0111487 | combined oxidative phosphorylation deficiency 7 | HGNC:26784 | Homo sapiens (human) | 91574 | MTRFR |
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| DOID:0110807 | hereditary spastic paraplegia 55 | HGNC:26784 | Homo sapiens (human) | 91574 | MTRFR |
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| DOID:0110326 | hypertrophic cardiomyopathy 20 | HGNC:29557 | Homo sapiens (human) | 91624 | NEXN |
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| DOID:0110424 | dilated cardiomyopathy 1CC | HGNC:29557 | Homo sapiens (human) | 91624 | NEXN |
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| DOID:0050768 | mitochondrial complex V (ATP synthase) deficiency nuclear type 1 | HGNC:18802 | Homo sapiens (human) | 91647 | ATPAF2 |
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| DOID:0111973 | immunodeficiency 17 | HGNC:1675 | Homo sapiens (human) | 917 | CD3G |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:5998 | Homo sapiens (human) | 9173 | IL1RL1 |
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| DOID:9408 | acute myocardial infarction | HGNC:5998 | Homo sapiens (human) | 9173 | IL1RL1 |
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| DOID:12662 | paracoccidioidomycosis | HGNC:5998 | Homo sapiens (human) | 9173 | IL1RL1 |
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| DOID:3393 | coronary artery disease | HGNC:5998 | Homo sapiens (human) | 9173 | IL1RL1 |
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| DOID:874 | bacterial pneumonia | HGNC:5998 | Homo sapiens (human) | 9173 | IL1RL1 |
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| DOID:0050156 | idiopathic pulmonary fibrosis | HGNC:5998 | Homo sapiens (human) | 9173 | IL1RL1 |
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| DOID:11266 | Hantavirus hemorrhagic fever with renal syndrome | HGNC:5998 | Homo sapiens (human) | 9173 | IL1RL1 |
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| DOID:0050865 | tongue squamous cell carcinoma | HGNC:5998 | Homo sapiens (human) | 9173 | IL1RL1 |
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| DOID:12554 | hemolytic-uremic syndrome | HGNC:5998 | Homo sapiens (human) | 9173 | IL1RL1 |
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| DOID:11166 | Human papillomavirus infectious disease | HGNC:5998 | Homo sapiens (human) | 9173 | IL1RL1 |
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